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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Accreditation
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (EPCAM, MLH1, MSH2, MSH6 and PMS2 genes ; MLH1 gene methylation ; microsatellites instability)
    • CHRU de Lille - Centre de Biologie Pathologie Génétique
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Accreditation
    • Molecular diagnosis of familial non polyposis colon cancer : search for mutations and big stature rearragements in MLH1, MSH2, MSH6, PMS2 genes
    • CLCC Institut Paoli Calmettes
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Heinrich-Heine-Universität Düsseldorf
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Labor Lademannbogen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of colon cancer, familial nonpolyposis predisposition (MLH1, MSH6, PMS2 and MSH2 genes)
    • CHU de Nantes - Institut de Biologie
    • Purpose(s) : Pre-symptomatic diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)
    • Ruhr-Universität Bochum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of Nonpolyposis colon cancer (MLH1, MSH2, MSH6, TACSTD1 genes)
    • University Hospitals Leuven - Gasthuisberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of colon cancer, familial nonpolyposis predisposition (MSH6, MLH1, MSH2 genes)
    • CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Accreditation
    • Molecular diagnosis of HNPCC- nonpolyposis colon cancer (MSH2, MLH1, MSH6 genes: mutation analysis)
    • Center for Medical Genetics Ghent
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Accreditation
    • Molecular diagnosis of Familial nonpolyposis colon cancer (MLH1 &MSH2 gene)
    • Erasme Hospital - ULB
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of hereditary non polyposis colon cancer (MLH1, MSH2, MSH6 and PMS2 genes : microsatellite instability)
    • Hôpitaux Universitaires de Genève HUG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer - HNPCC (MLH1, MSH2 and MSH6 genes: mutation scanning by bi-directional DNA sequence analysis)
    • St Mary's Hospital
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer - HNPCC (MLH1, MSH2, MSH6 genes)
    • Liverpool Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer (HNPCC). For MSI studies, paraffin blocks from tumour are required - please discuss with laboratory before sending (MSH2, MLH1, MSH6, PMS2 genes)
    • Birmingham Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6 genes/ microsatellite instability)
    • Mitteldeutscher Praxisverbund Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer (HNPCC, MSI analysis and MLH, MSH2 and MSH6 genes: Sequencing and dosage analysis)
    • University Hospital of Wales
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Hereditary Nonpolyposis Colorectal Cancer - HNPCC (hMLH1, hMSH2 and hMSH6: by DHPLC and sequencing)
    • Salisbury District Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Wiltshire
    • SALISBURY
    • Accreditation
    • Molecular diagnosis of Hereditary Non Polyposis Colon Cancer - HNPCC, Lynch syndrome (MLH1 gene sequence analysis and MSI analysis of tumour tissue)
    • Ninewells Hospital and Medical School
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Tayside
    • DUNDEE
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer - HNPCC (MLH1, MSH2 & MSH6 genes)
    • North West London Hospitals NHS - Northwick Park & St Marks Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Greater London
    • HARROW
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Zentrum für Humangenetik Mannheim
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2 and MSH6 genes)
    • Medizinisches Versorgungszentrum Humane Genetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Universitätsklinikum Regensburg
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Accreditation
    • Molecular diagnosis of Hereditary Non-Polyposis Colorectal Cancer (MLH1, MSH2, MSH6 and PMS2 gene and search for microsatellite instability)
    • VUmc - VU medisch centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Hereditary Non-Polyposis Colorectal Cancer (MLH1, MSH2, MSH6 and PMS2 gene)
    • LUMC - Leids Universitair Medisch Centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • LEIDEN
    • Accreditation
    • Molecular diagnosis of Lynch Syndrome (MLH1, MSH2, MSH6 and PMS2 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular Diagnosis of Colon cancer, familial nonpolyposis. APC gene
    • Laboratorio de Análisis Dr. Echevarne
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Accreditation
    • Molecular diagnosis of Familial nonpolyposis colon cancer (MLH1 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Hereditary Non-Polyposis Colorectal Cancer (MLH1, MSH2, MSH6 and PMS2 gene)
    • AMC - Academisch Medisch Centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Diagnosis of the colon cancer familial nonpolyposis (MLH1, MSH2, MSH6, PMS2, EPCAM genes)
    • Hospital General Universitario de Elche
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Methylation analysis, Deletion / Duplication analysis
    • Technical procedure(s) : Sanger sequencing, MLPA based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ELCHE
    • Accreditation
    • Molecular diagnosis of Hereditary Non-Polyposis Colon Cancer (MSH2 and MSH6 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PIK3CA, PMS2 genes)
    • Praxis für Humangenetik Freiburg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of nonpolyposis colon cancer (PPARG gene)
    • Praxis Dr. Mato Nagel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Accreditation
    • Molecular diagnosis of Lynch Syndrome (HNPCC) and Familial Colorectal Cancer (MLH1 or MSH2 genes: Testing for known mutations in family members)
    • International Centre for Life
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer - HNPCC (MLH1, MSH2 and MSH6 genes: mutation screening by sequencing and dosage analysis by MLPA)
    • The Churchill Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer - HNPCC (MLH1, MSH2 and MSH6: DNA sequencing and dosage)
    • Addenbrooke's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Molecular diagnosis of nonpolyposis colon cancer (MSH6 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PIK3CA, PMS2 genes; microsatellite instability testing)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of Hereditary Non-Polyposis Colorectal Cancer (MLH1, MSH2, MSH6 gene and search for microsatellite instability)
    • Erasmus MC, Faculteitsgebouw
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Accreditation
    • Molecular diagnosis of Hereditary Non-Polyposis Colorectal Cancer (EPCAM, MLH1, MSH2, MSH6 and PMS2 gene, Microsatellite Instability and MLH1 promotormethylation)
    • UMCG - Universitair Medisch Centrum Groningen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • NETHERLANDS
    • Groningen
    • GRONINGEN
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer - HNPCC (MSH2, MLH1, MSH6: DNA sequencing; MSH2 and MLH1: MLPA dosage)
    • Sheffield Children's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer HNPCC (MLH1, MSH2, MSH6 & PMS2 genes)
    • Université Catholique de Louvain - UCL
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUXELLES
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (EPCAM, MLH1, MSH2, MSH6, PMS1, PMS2 genes)
    • Centogene AG
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MLH3, MSH2, MSH6, PMS1, PMS2 genes: sequencing, MLPA)
    • Universitätsklinikum Ulm
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2 genes)
    • MVZ Labor Dr. Reising-Ackermann und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • LEIPZIG
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes : sequencing/ MLPA/ microsatellite analysis)
    • Diagenom GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Medizinisch Genetisches Zentrum München
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)
    • Medizinische Hochschule Hannover
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Accreditation
    • Molecular screening for HNPCC - nonpolyposis colon cancer (MSI analysis)
    • Center for Medical Genetics Ghent
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MLH3, MSH2, MSH6, PMS1, PMS2 genes)
    • Paxis und Labor Dr. med Karl Mehnert
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • NEU-ULM
    • Accreditation
    • Molecular diagnosis of Hereditary Nonpolyposis Colorectal Cancer (MLH1, MSH2 and MSH6 gene)
    • AZM - Academisch Ziekenhuis Maastricht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2 and MSH6 genes: microsatellite instability)
    • Sahlgrenska university hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWEDEN
    • Västra Götalandsregionen
    • GÖTEBORG
    • Accreditation
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (Sequencing: MLH1, MSH2, MSH6; MLPA: MLH1, MSH2; microsatellite instability)
    • Asper Biotech Ltd.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing, MLPA based techniques
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colorectal Cancer -HNPCC (MLH1, MSH2 and MSH6 genes: sequencing and MLPA)
    • Nottingham City Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • Nottinghamshire
    • NOTTINGHAM
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Universitätsmedizin Mainz
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Accreditation
    • Molecular diagnosis of Hereditary nonpolyposis colon cancer (by MSI, BRAF and acquired KRAS mutation testing)
    • Southmead Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (microsatellite instability in tumor tissue)
    • Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS1, PMS2, EPCAM, and TGFBR2 genes)
    • Medizinische Universität Graz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Accreditation
    • Molecular diagnosis of Lynch syndrome (MLH1, MSH2, MSH6, PMS1, PMS2, EPCAM, and TGFBR2 gene)
    • Medizinische Universität Graz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1 and MSH2 genes)
    • Centrum für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Hessen
    • BAD NAUHEIM
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (microsatellites, MLH1, MSH2, MSH6, PMS1, PMS2 genes)
    • MVZ Fenner & Krasemann
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS1, PMS2 genes)
    • Labor PD Dr. Volkmann und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • KARLSRUHE
    • Accreditation
    • Preimplantation molecular diagnosis of Hereditary Non Polyposis Colon Cancer - HNPCC, Lynch syndrome (MLH1 and MSH2: by linkage and mutation analysis)
    • Institute for Women's Health
    • Purpose(s) : Pre-implantation diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of hereditary nonpolyposis colorectal cancer (MLH1, MSH2 and MSH6 genes: all exons including intron bounderies ; microsatellite instability)
    • Onkologicky ustav sv. Alzbety s.r.o.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2 and MSH6 genes)
    • GenteQ GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of Lynch Syndrome (by Sanger sequencing- coding region MLH1, MSH2, MSH6)
    • Trillium Health Partners- Credit Valley Site
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : Sanger sequencing
    • More information
    • CANADA
    • Ontario
    • MISSISSAUGA
    • Accreditation
    • Molecular diagnosis of Lynch syndrome (MLH1, MSH2, MSH6, and PMS2 genes)
    • Medizinische Universität Innsbruck
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Accreditation
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes: entire coding region)
    • Unilabs Lausanne
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of Muir-Torre Syndrome (MLH1, MSH2 genes)
    • Birmingham Women's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Universität Würzburg - Biozentrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, BRAF genes / Sequence analysis: select exons, Methylation analysis, MLPA)
    • Hospital General Universitario de Elche
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ELCHE
    • Accreditation
    • Molecular diagnosis of Lynch syndrome (hereditary colon cancer) (MLH1, MSH2, MSH6, PMS2, EPCAM genes)
    • Universität Zürich
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular Diagnosis of Hereditary Colon Cancer (MLH1, MSH2 sequencing and MLPA)
    • Children's Hospital of Eastern Ontario
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • CANADA
    • Ontario
    • OTTAWA
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)
    • Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (EPCAM, MLH1, MSH2, MSH6, PMS2 genes: sequencing)
    • Pränatalmedizin München
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular Diagnosis of Lynch Syndrome (MLH1, MSH2, MSH6 sequencing and MLPA, EPCAM MLPA, IHC and MSI)
    • Mount Sinai Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)
    • Universitätsklinikum Schleswig-Holstein - Campus Kiel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Schleswig-Holstein
    • KIEL
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (EPCAM, MLH1, MSH2, MSH6, PMS2 genes)
    • Institut für Humangenetik der Universität Göttingen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing, MLPA based techniques
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)
    • laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of HNPCC (EPCAM, MLH1, MSH2, MSH6, PMS2 genes)
    • Synlab Lausanne
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)
    • Institut für Humangenetik am Universitätsklinikum Heidelberg
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer, HNPCC (sequence and MLPA dosage analysis of MLH1, MSH2, MSH6 & PMS2 genes)
    • St James's University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • Accreditation
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Institut für angewandte Humangenetik und Onkogenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • BAD STEBEN
    • Accreditation
    • Molecular diagnosis of Turcot syndrome (PMS2 gene)
    • St James's University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • Accreditation
    • Molecular TherapID KRAS mutation test
    • DNA VISION SA
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Familial Non Polyposis Colorectal Cancer -HNPCC (MLH1, MSH2 and MSH6 genes: sequencing and MLPA)
    • Belfast City Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • UNITED KINGDOM
    • Antrim and Newtownabbey
    • BELFAST
    • Accreditation
    • Molecular Diagnosis of Hereditary Nonpolyposis Colon Cancer (MSH2 c.942+3A>T mutation)
    • Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Terre-Neuve-et-Labrador
    • ST. JOHN'S
    • Accreditation
    • Molecular Diagnosis of Hereditary Cancer Predisposition - Comprehensive NGS Panel (25 genes)
    • London Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • CANADA
    • Ontario
    • LONDON
    • Accreditation
    • Molecular Diagnosis of High Penetrance Hereditary Cancer Predisposition - Comprehensive NGS Panel (16 genes)
    • London Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • CANADA
    • Ontario
    • LONDON
    • Accreditation
    • Molecular Diagnosis of Colorectal/Gastric Hereditary Cancer Predisposition - Comprehensive NGS Panel (15 genes)
    • London Health Sciences Centre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • CANADA
    • Ontario
    • LONDON
    • Accreditation
    • Molecular Diagnosis of Lynch Syndrome- Comprehensive NGS Panel (4 genes) and del/dup (4 genes plus EPCAM)
    • Toronto General Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES), MLPA based techniques
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Accreditation
    • Molecular Diagnosis of Lynch Syndrome (MLH1 methylation in blood)
    • Toronto General Hospital
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Molecular diagnosis of familial nonpolyposis colon cancer (HNPCC syndrome)
    • Faculté de médecine et de pharmacie de Rouen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Predisposition molecular diagnosis of familial nonpolyposis colon cancer (MSH2 and MLH1 genes)
    • CLCC Institut Bergonié
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of nonpolyposis colon cancer (MLH1, MSH2, MSH6 and PMS2 genes)
    • CLCC Léon Bérard
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing, PCR based techniques, MLPA based techniques
    • More information
    • FRANCE
    • RHONE-ALPES
    • LYON
    • Molecular diagnosis of nonpolyposis colon cancer (MSH2, MLH1, MSH6 genes)
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of nonpolyposis colon cancer : hMSH2, hMSH6, hMLH1 genes and RER phenotype
    • CHRU de Montpellier - Hôpital Arnaud de Villeneuve
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Search for RER phenotype in colon cancer
    • CHU de Strasbourg - Hôpital de Hautepierre
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ALSACE
    • STRASBOURG
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MLH3, MSH2, MSH6 genes, microsatellite analysis)
    • Biotecnologie Avanzate Srl
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MSH2, MLH1, MSH6 genes determined by sequence analysis of the entire coding region and MLPA)
    • Centro di Riferimento Oncologico
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : MLPA based techniques
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • AVIANO
    • Molecular diagnosis of familial nonpolyposis colon cancer (microsatellites, MLH1, MSH2, MSH6, MLH3, PMS1, PMS2 genes)
    • Laborärztlich-humangenetische Partnerschaft Eiben - Glaubitz
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH6 genes)
    • Medizinische Universität Graz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Molecular diagnosis of predisposition to colon cancer (MLH1, MSH2 and MSH6 genes)
    • CHU de Nancy - Hôpital de Brabois
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Methylation analysis
    • Technical procedure(s) : Sanger sequencing, MLPA based techniques
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LÈS-NANCY
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6 and PMS2 genes / deletions and duplications)
    • Hospital Universitario Virgen del Rocío
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2 and MSH6 genes)
    • Centro de Diagnóstico Biomédico - CDB
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of nonpolyposis colon cancer (MLH1 and MSH2 genes)
    • CHU Paris Centre - Hôpital Cochin
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • 'Immunohistochemistry and molecular diagnosis of familial nonpolyposis colon cancer (Lynch syndrome or HNPCC; MSH2, MSH6, PMS2, MLH1 genes)'
    • A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Biochemical genetics
    • Objective(s) : Protein expression
    • Technical procedure(s) : Immunohistochemistry
    • More information
    • ITALY
    • LOMBARDIA
    • VARESE
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2 genes)
    • Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of Hereditary Non Polyposis Colorectal Cancer (HNPCC)
    • Universitätsspital Basel
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BASEL
    • Colon cancer, familial, non polyposis : microsatellites anomalies research (MLH1 and MSH2 genes)
    • CHU Paris Seine-Saint-Denis - Hôpital Avicenne
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • BOBIGNY
    • Molecular diagnosis of familial nonpolyposis colon cancer (HNPCC) and search for microsatellites instabilities
    • CLCC Institut Curie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of nonpolyposis colon cancer (MLH1 gene)
    • Oulu University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FINLAND
    • Finland
    • OULU
    • Molecular diagnosis of familial nonpolyposis colon cancer (search for microsatellite instabilities and MLH1, MSH2 and MSH6 genes)
    • CLCC Institut Gustave Roussy
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Uniparental disomy study, Deletion / Duplication analysis
    • Technical procedure(s) : Sanger sequencing, MLPA based techniques
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • VILLEJUIF
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • Universitätsklinikum Bonn
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of colon cancer familial nonpolyposis (MLH1, MSH2, MSH6, PMS2 genes)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 and PMS2 gene sequencing and MLPA)
    • Aarhus Universitetshospital - Skejby
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • DENMARK
    • Jylland
    • AARHUS
    • Molecular diagnosis of HNPCC syndrome (EPCAM, MLH1, MLH3, MSH2, MSH6, PMS1, PMS2, TGFBR2 genes)
    • Praxis Dres. Gencik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 and EPCAM genes)
    • IUCT Oncopole - CLCC Institut Claudius Regaud
    • Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : Sanger sequencing, MLPA based techniques
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Screening of nonpolyposis colon cancer : protein immunohistochemical analyses
    • CLCC Institut Gustave Roussy
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Biochemical genetics
    • Objective(s) : Protein expression
    • Technical procedure(s) : Immunohistochemistry
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • VILLEJUIF
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MSH2, MSH6, MLH1, EPCAM genes)
    • CHU de Strasbourg - Hôpital Civil
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ALSACE
    • STRASBOURG
    • Molecular diagnosis of hereditary nonpolyposis colorectal cancer (MLH1, MSH2 and MSH6 genes)
    • Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of nonpolyposis colon cancer (MSH2, MLH1, MSH6 and PMS2 genes, and microsatellite analysis)
    • Instituto Português de Oncologia do Porto, EPE / IPOFG - CRO Porto
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of familial nonpolyposis colon cancer. KRAS gene
    • Hospital Regional Universitario de Málaga - Hospital General
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of Hereditary non-polyposis colorectal cancer (MLH1, MSH2 and MSH6 gene; search for microsatellite instability and methylation of MLH1 promoter)
    • Het Nederlands Kanker Instituut - Antoni van Leeuwenhoek Ziekenhuis
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 and PMS2 genes)
    • Centro de Bioquímica y Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Murcia
    • EL PALMAR
    • Molecular diagnosis of Familial Non Polyposis Colon Cancer - HNPCC (MSH2 and MSH6 genes)
    • Western General Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Molecular diagnosis of the familial nonpolyposis colon cancer (MLH1, MSH2 MSH6, PMS1 y PMS2 genes)
    • Sistemas Genómicos S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of proneness to familial nonpolyposis colon cancer (MSH2 and MLH1 genes)
    • Laboratorio Genoma
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Institut für Humangenetik des Universitätsklinikums Münster
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • Consorzio per la Genetica Molecolare Umana
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MONZA
    • Molecular diagnosis of familial non polyposis colon cancer (APC gene)
    • Karolinska University Hospital - Clinical Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of familial non polyposis colon cancer (MLH1, MSH2, MSH6 and PMS2 genes)
    • Karolinska University Hospital - Clinical Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of hereditary nonpolyposis colorectal cancer (microsatellite instability; MLH1 promoter methylation detected by methylation-senstivie MLPA)
    • Sygehus Lillebaelt Vejle Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • DENMARK
    • Syddanmark
    • VEJLE
    • Immunohistochemical and molecular diagnosis of HNPCC syndrome (MLH1, PMS2, MSH2, MSH6 genes and microsatellite analysis)
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Biochemical genetics
    • Objective(s) : Protein expression
    • Technical procedure(s) : Immunohistochemistry
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of the familial nonpolyposis colon cancer (MSH2, MSH6, MLH1, PMS2 genes)
    • INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of hereditary non polyposis colon cancer (MLH1, MSH2 and MSH6 genes)
    • CLCC Jean Perrin
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • AUVERGNE
    • CLERMONT-FERRAND
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes: sequencing / MLPA)
    • Pränatalzentrum Hamburg und Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Molecular diagnosis of familial nonpolyposis colon cancer (EPCAM, MLH1, MSH2, MSH6, PMS2 genes: sequencing / MLPA)
    • Praxis für Humangenetik und Prävention
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of colon cancer, familial nonpolyposis (microsatellite inestability; large deletions by MLPA kit P003, MLPA kit ME011; entire coding sequence of MLH1, MSH2 and MSH6 genes; BRAF gene / mutation V600E)
    • Hospital Universitario Donostia
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of colon cancer, familial nonpolyposis(MSH2, MLH1, PMS2 genes)
    • Genetaq
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis MLH1 and MSH2-related hereditary nonpolyposis colorectal cancer: microsatelite instability analysis
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of hereditary nonpolyposis colorectal cancer (RER phenotype; p.V600E mutation in the BRAF gene)
    • CHRU de Brest - Hôpital Morvan
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular diagnosis of hereditary nonpolyposis colorectal cancer (MLH1, MSH2, MSH6, BRAF and KRAS genes)
    • Faculdade de Medicina da Universidade de Lisboa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (entire coding sequence of MLH1, MSH2 and MSH6 genes)
    • Lorgen G.P.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Preimplantation genetic diagnosis of hereditary nonpolyposis colon cancer (MSH2 gene)
    • Reprogenetics Spain S.A.
    • Purpose(s) : Pre-implantation diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH6, MSH2, PMS1, PMS2 genes / entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2 and MSH6 genes - sequencing/MLPA)
    • ICO L'Hospitalet
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes)
    • Klinikum Stuttgart - Standort Olgahospital
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes: sequencing / MLPA)
    • Gemeinschaftspraxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6, KRAS, PIK3CA genes; microsatellite instability analysis)
    • Azienda Ospedaliera Istituti Ospitalieri di Cremona
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • CREMONA
    • Preimplantation genetic diagnosis of hereditary nonpolyposis colon cancer (MSH2 and MSH6 genes)
    • CME Barcelona
    • Purpose(s) : Pre-implantation diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • IBGM - Instituto de Biología y Genética Molecular
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Castilla - León
    • VALLADOLID
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • Hospital Clínico San Carlos
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • La Rioja
    • LOGROÑO
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2 and MSH6 genes)
    • Institut für Humangenetik am Universitätsklinikum Leipzig
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • LEIPZIG
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (sequencing of MSH6, MSH2 and MLH1 genes)
    • Onkologikoa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2 and MSH6 genes)
    • MVZ wagnerstibbe für Laboratoriumsmedizin und Pathologie GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (microsatellite instability - 5 markers)
    • Hospital Universitario Virgen del Rocío
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of hereditary colon cancer (MUTYH, EPCAM, MSH2, MSH6, MLH1, APC, BMPR1A, PTEN, MLH3, SMAD4, STK11 genes / array-CGH)
    • Policlínica Gipuzkoa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : Array based techniques
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2, KRAS genes)
    • Consorci Sanitari de Terrassa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • TERRASSA
    • Molecular diagnosis of EPCAM-related Lynch syndrome (EPCAM gene: sequencing of the entire coding region and deletion/duplication analysis)
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of hereditary nonpolyposis colorectal cancer (MLH1, MSH2, MLH3, MSH6, BMPR1 and PMS2 genes: Sequencing of the entire coding region for MLH1, MSH2, MLH3, MSH6, BMPR1 genes and deletion/duplication analysis by MLPA for MLH1, MSH2, MSH6 and PMS2 genes)
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS1, PMS2 genes: entire coding sequence; MLH1, MSH2 genes: MLPA)
    • Centro Inmunológico de Alicante (CIALAB)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes / sequencing)
    • Universidad de Salamanca. Facultad de Medicina
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of Lynch Syndrome (HNPCC) and Familial Colorectal Cancer by sequencing of the entire coding region of the gene(s) plus copy number analysis (Genes: MSH2, MSH6)
    • Western General Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Molecular diagnosis of Hereditary non-polyposis colorectal cancer (NGS panel for MLH1, MSH2, MSH6 PMS2 and EPCAM genes: Sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Methylation analysis of the MLH1 gene promotor by ms-MLPA
    • CGC Genetics / Centro de Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MSH2, MSH6, PMS2 genes / PCR, gene sequencing, MLPA, capillary electrophoresis; microsatellite instability in tumor tissue / PCR, capillary electrophoresis; MLH1 gene / bisulfite methylation PCR)
    • IMOMA - Instituto de Medicina Oncológica y Molecular de Asturias
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • Technical procedure(s) : PCR based techniques, MLPA based techniques
    • More information
    • SPAIN
    • Asturias
    • OVIEDO
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • Hospital del Mar
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular Diagnosis of Hereditary Non-Polyposis Colorectal Cancer (MLPA, sequencing, targeted mutation analysis MLH1, MSH2, MSH6, PMS2)
    • University of Alberta
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • CANADA
    • Alberta
    • EDMONTON
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (EPCAM gene / MLPA)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2 genes: sequencing / MLPA)
    • Institut für Humangenetik der Universitätsmedizin Greifswald
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • GREIFSWALD
    • Molecular and immunohistochemical diagnosis of hereditary nonpolyposis colon cancer (microsatellites instability analysis for: BAT25, BAT26, D2S123, D17S250, DS346, BAT40, NR21, NR24, D18S58, TGFBR2 - immunohistochemical analysis of MLH1, MSH2, MSH6 proteins)
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS2, EPCAM genes)
    • Bioarray
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : NGS sequencing (except WES), MLPA based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ELCHE
    • Molecular diagnosis of HNPCC syndrome (MLH1, MSH2, MSH6, PMS2 genes)
    • Humangenetisches Institut am Universitätsklinikum Erlangen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • ERLANGEN
    • Molecular diagnosis of familial nonpolyposis colon cancer (hMLH1, hMSH2, hMSH6 genes)
    • IRCCS "Saverio De Bellis"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • CASTELLANA GROTTE
    • Molecular diagnosis of familial adenomatous polyposis (MLH1, MSH2, MSH6, MYH genes)
    • Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • BARI
    • Molecular diagnosis of Turcot syndrome (APC, MSH2, MLH1 genes)
    • Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • BARI
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • BARI
    • Molecular diagnosis of Muir-Torre syndrome (MSH2 gene)
    • Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • BARI
    • Molecular diagnosis of colon cancer, familial nonpolyposis (microsatellite instability)
    • CHRU de Tours - Hôpital Trousseau
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • CENTRE
    • TOURS
    • Molecular diagnosis of familial nonpolyposis colon cancer
    • Alborg Sygehus Nord
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • DENMARK
    • Jylland
    • ALBORG
    • Molecular diagnosis of nonpolyposis colon cancer. MSH2, MLH1, MSH6 genes
    • Hospital Universitario Cruces - Osakidetza
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • País Vasco
    • BARAKALDO
    • Molecular diagnosis of nonpolyposis colon cancer (MLH1 and MSH6 genes)
    • BIOGENOMICA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of familial nonpolyposis colon cancer (MSH6 gene)
    • Azienda Ospedaliero-Universitaria San Luigi Gonzaga
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PIEMONTE
    • ORBASSANO
    • Molecular diagnosis of nonpolyposis colon cancer
    • Análisis Genéticos ANCOR S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ALICANTE
    • Molecular diagnosis of colon cancer, familial nonpolyposis (MLH1, MSH2 and MSH6 genes)
    • Azienda Ospedaliero Universitaria Careggi - NEUROFARBA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Molecular diagnosis of nonpolyposis colon cancer
    • Istituto Nazionale per la Ricerca sul Cancro - IST
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6, PMS1 and PMS2 genes)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Molecular diagnosis of familial nonpolyposis colon cancer
    • Albrecht-Kossel-Institute for Neuroregeneration (AKos)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Predisposition molecular diagnosis of familial nonpolyposis colon cancer (MSH2 and MLH1 genes)
    • Motol university hospital - 2nd Medical School Charles University Prague
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Predisposition molecular diagnosis of familial nonpolyposis colon cancer
    • Acibadem healthcare group
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of predisposition to familial nonpolyposis colon cancer (MSI)
    • GeneticLab
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • More information
    • ROMANIA
    • BUCURESTI
    • BUCURESTI
    • Molecular diagnosis of susceptibility to familial nonpolyposis colon cancer (MLH1, MSH2 and MSH6 gene analysis by sequencing and MLPA)
    • Amplexa Genetics A/S
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • DENMARK
    • Fyn
    • ODENSE
    • Molecular diagnosis of familial non polyposis colon cancer (PMS1, PMS2, MLH1, MSH2, MSH6 genes)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of Hereditary Non-Polyposis Colorectal Cancer (MSH2, Mutation analysis)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Colon cancer (APC, MSH2, Mutation analysis, PGD)
    • Sheba Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ISRAEL
    • ISRAEL
    • RAMAT GAN
    • Molecular diagnosis of Colon Cancer (MSH2, Mutation analysis)
    • Rabin Medical Center - Beilinson Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ISRAEL
    • ISRAEL
    • PETAH TIKVA
    • Molecular diagnosis of Colon Cancer, HNPCC (MSH2, Mutation analysis)
    • Shaare Zedek Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of familial nonpolyposis colon cancer (Microsatellite instability analysis, methylation analysis of MLH1 gene and mutation analyses of BRAF, MLH1, MSH2 and MSH6 genes)
    • IB Genetics OÜ
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Methylation analysis
    • More information
    • ESTONIA
    • Tallinn
    • TALLINN
    • Molecular diagnosis of familial non polyposis colon cancer (MLH1, MSH2 and MSH6 genes)
    • Oslo Universitetssykehus HF, Rikshospitalet
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NORWAY
    • Østlandet
    • OSLO
    • Molecular diagnosis of colon cancer (KRAS gene)
    • Azienda Ospedaliera San Giuseppe Moscati
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • CAMPANIA
    • AVELLINO
    • Molecular diagnosis of hereditary nonpolyposis colorectal cancer (MLH1, MSH2 and MSH6 genes: full sequencing and screening of large genomic rearrangements by MLPA)
    • National center for scientific research Demokritos
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Diagnosis of Lynch syndrome (MSH2 gene; NR21, NR24, NR22, BAT 25, BAT26 markers)
    • CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Saint-Louis
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of colon cancer, familial nonpolyposis (MSH2, MSH6 and MLH1 genes)
    • Centro Nacional de Investigaciones Oncológicas (CNIO)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of familial nonpolyposis colon cancer
    • IRST - Istituto Scientifico Romagnolo per lo studio e la cura dei Tumori
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • MELDOLA
    • Molecular diagnosis of familial nonpolyposis colon cancer (MSH2 gene)
    • Masaryk Memorial Cancer Institute
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CZECH REPUBLIC
    • South Moravia
    • BRNO
    • Molecular diagnosis of hereditary non-polyposis colorectal cancer (MLH1, MSH2, MSH6 and PMS2 genes)
    • Pronto Diagnostics Ltd.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ISRAEL
    • ISRAEL
    • TEL AVIV
    • Postnatal molecular diagnosis of familial nonpolyposis colon cancer (MLH1 and MSH2 genes:deletion/duplication analysis by MLPA)
    • National institute of legal medicine
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • ROMANIA
    • BUCURESTI
    • BUCURESTI
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (entire coding sequence of MLH1, MSH2, MSH6, PMS1 and PMS2 genes; deletions of MLH1 and MSH2 genes by MLPA analysis; microsatellite instability: BAT25, BAT26, D5S346, D17S250, D2S123, NR21, NR22 and NR24)
    • Laboratorio de Genética Clínica, S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1 and MSH2)
    • INCLIVA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1 and MSH2 genes)
    • Hospital San Pedro
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • La Rioja
    • LOGROÑO
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (sequencing of MLH1, MSH2, MSH6 and PMS2 genes)
    • Genyca Innova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MAJADAHONDA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes)
    • Ospedale "R. Binaghi"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Molecular diagnosis of predisposition to hereditary non polyposis colon cancer (MLH1, MSH2 genes)
    • USI - Unione Sanitaria Internazionale
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2, MSH6 genes / microsatellite instability - 5 markers)
    • Hôpital général juif - Jewish General Hospital
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • Molecular diagnosis of cancer (NGS Cancer Panel)
    • ATG GenMed GmbH
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Preimplantation genetic diagnosis of hereditary nonpolyposis colon cancer (MLH1, MSH2 genes)
    • Igenomix Spain
    • Purpose(s) : Pre-implantation diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of colon cancer (KRAS gene)
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2 genes)
    • Presidio Ospedaliero "Vito Fazzi" - ASL LE
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • LECCE
    • Molecular diagnosis of familial nonpolyposis colon cancer (MLH1 and MSH2 genes: sequencing)
    • ATG GenMed GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Microsatelite instability for colorectal cancer syndromes
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Analysis for known mutations f colorectal cancer syndromes (hMLH1 3p22.2)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Mutation screening of colorectal cancer syndromes (hMLH1 3p22.2)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Analysis for known mutations of colorectal cancer syndromes (hMSH2 2p21)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Mutation screening of colorectal cancer syndromes (hMSH2 2p21)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Mutation screening of colorectal cancer syndromes (hPMS1 2q32.2)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Analysis of known mutations for colorectal cancer syndromes (hPMS1 2q32.2)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Analysis of known mutations for colorectal cancer syndromes (hPMS2 7p22.1)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Mutation screening for colorectal cancer syndromes (hPMS2 7p22.1)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Mutation screening for colorectal cancer syndromes (hMSH6 2p16.3)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Analysis of known mutations for colorectal cancer syndromes (hMSH6 2p16.3)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Analysis of known mutations for colorectal cancer syndromes (MYH 1p34.1)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Mutation screening for colorectal cancer syndromes (MYH 1p34.1)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Immunohistochemistry for colorectal cancer syndromes (hMLH1 3p22.2)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Immunohistochemistry for colorectal cancer syndromes (hMSH2 2p21)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Immunohistochemistry for colorectal cancer syndromes (hMLH6)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Immunohistochemistry for colorectal cancer syndromes (hPMS2 7p22.1)
    • The Cyprus Institute of Neurology and Genetics
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA