Search for a diagnostic test
159 Result(s)
Caption
: Accreditation
= ;

BRETAGNE
RENNES
Molecular diagnosis familial adenomatous polyposis (APC and MUTYH gene mutations and rearrangements)
CHU de Rennes - Hôpital Pontchaillou
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

HAUTS-DE-FRANCE
LILLE
Molecular diagnosis of familial adenomatous polyposis including Gardner syndrome (APC, MUTYH genes)
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Bayern
MÜNCHEN
Molecular diagnosis of familial adenomatous polyposis (APC, AXIN2 and MUTYH genes)
Medizinisch Genetisches Zentrum München
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
Predisposition to familial adenomatous polyposis : search for germinal mutations in APC and MUTYH 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, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

OOST-VLAANDEREN
GENT
Molecular diagnosis of Familial adenomatous polyposis (APC & MYH genes)
Center for Medical Genetics Gent
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Erasme Hospital - ULB
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Suisse Romande
GENÈVE
Molecular diagnosis of familial adenomatous polyposis (APC and MYH genes)
Hôpitaux Universitaires de Genève HUG
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

STEIERMARK
GRAZ
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Medizinische Universität Graz
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

West Midlands
BIRMINGHAM
Molecular diagnosis of Familial Adenomatous Polyposis including sequencing of MYH Polyposis common mutations (APC and MUTYH genes)
Birmingham Women's NHS Foundation Trust
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

Sachsen
DRESDEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Mitteldeutscher Praxisverbund Humangenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

South Glamorgan
CARDIFF
Molecular diagnosis of Familial Adenomatous Polyposis (APC and MUTYH genes: Molecular diagnosis through sequencing analysis)
University Hospital of Wales
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics, Cytogenetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis, Detection of microdeletions/microduplications
Technique(s)
: NGS sequencing (except WES), MLPA based techniques

Baden-Württemberg
MANNHEIM
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Zentrum für Humangenetik Mannheim
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Bayern
MÜNCHEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Zweigniederlassung der synlab MVZ Augsburg GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Bayern
REGENSBURG
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Universitätsklinikum Regensburg
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Zuid-Holland
LEIDEN
Molecular diagnosis of Familial Adenomatous Polyposis (APC gene)
LUMC - Leids Universitair Medisch Centrum
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Noord-Holland
AMSTERDAM
Molecular diagnosis of Familial Adenomatous Polyposis (APC gene)
AMC - Academisch Medisch Centrum
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

OCCITANIE
MONTPELLIER
Molecular preimplantation genetic diagnosis of familial adenomatous polyposis (APC gene: targeted mutation analysis)
IURC - Institut Universitaire de Recherche Clinique
Purpose(s)
: Pre-implantation diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

Zuid-Holland
ROTTERDAM
Molecular diagnosis of Familial Adenomatous Polyposis (MUTYH, BMPR1A, NTHL1, SMAD4 and APC gene)
Erasmus MC, Faculteitsgebouw
Purpose(s)
: Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Oxfordshire
OXFORD
Molecular diagnosis of Familial Adenomatous Polyposis (APC: 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
Technique(s)
: MLPA based techniques

Baden-Württemberg
FREIBURG
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Praxis für Humangenetik Freiburg
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Mecklenburg-Vorpommern
ROSTOCK
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Centogene AG
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Baden-Württemberg
ULM
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes: sequencing, MLPA)
Universitätsklinikum Ulm
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Sachsen
LEIPZIG
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
MVZ Labor Dr. Reising-Ackermann und Kollegen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Mecklenburg-Vorpommern
ROSTOCK
Molecular diagnosis of familial adenomatous polyposis (APC gene: sequencing / MLPA; MUTYH gene: complete sequencing)
Diagenom GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

AUVERGNE-RHONE-ALPES
CLERMONT-FERRAND
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
CLCC Jean Perrin
Purpose(s)
: Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, PCR based techniques, MLPA based techniques

Hamburg
HAMBURG
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes: sequencing, MLPA)
Labor Lademannbogen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Nordrhein-Westfalen
DÜSSELDORF
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Heinrich-Heine-Universität Düsseldorf
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Comunidad Valenciana
ELCHE
Diagnosis of the familial adenomatous polyposis (MUTYH and APC genes)
Hospital General Universitario de Elche
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUXELLES
Molecular diagnosis of Familial adenomatous polyposis (APC & MYH genes)
Université Catholique de Louvain - UCL
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Tartu
TARTU
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Asper Biogene
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Bayern
NEU-ULM
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Paxis und Labor Dr. med Karl Mehnert
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Baden-Württemberg
HEIDELBERG
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Institut für Humangenetik am Universitätsklinikum Heidelberg
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Nordrhein-Westfalen
DORTMUND
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Murcia
EL PALMAR
Diagnosis of familial adenomatous polyposis (APC gene)
Centro de Bioquímica y Genética Clínica
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

Wiltshire
SALISBURY
Molecular diagnosis of familial adenomatous polyposis (MYH gene: 2 common mutations by sequencing)
Salisbury District Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

Rheinland-Pfalz
INGELHEIM AM RHEIN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Tayside
DUNDEE
Molecular diagnosis of Familial adenomatous polyposis - FAP (APC gene: sequence analysis and deletion testing by MLPA)
Ninewells Hospital and Medical School
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Deletion / Duplication analysis
Technique(s)
: MLPA based techniques

Nordrhein-Westfalen
KÖLN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Gelderland
NIJMEGEN
Molecular diagnosis of Familial Adenomatous Polyposis (APC gene)
Radboudumc - Radboud universitair medisch centrum
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Hamburg
HAMBURG
Molecular diagnosis of familial adenomatous polyposis (APC gene)
MVZ Fenner & Krasemann
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

TIROL
INNSBRUCK
Molecular diagnosis of familial adenomatous polyposis and attenuated familial adenomatous polyposis (APC and MUTYH genes)
Medizinische Universität Innsbruck
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

Baden-Württemberg
KARLSRUHE
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Labor PD Dr. Volkmann und Kollegen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Rheinland-Pfalz
MAINZ
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Universitätsmedizin Mainz
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of intestinal polyposis syndrome (gene panel)
Reference Laboratory Genetics
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

Suisse Alémanique
SCHLIEREN
Molecular diagnosis of polyposis syndromes (gene panel APC, STK11, SMAD4, BMPR1A)
Universität Zürich
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Bayern
MARTINSRIED
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Bayern
MÜNCHEN
Molecular diagnosis of familial adenomatous polyposis (APC, AXIN2, MUTYH genes: sequencing / MLPA)
Pränatalmedizin München
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Niedersachsen
HANNOVER
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Medizinische Hochschule Hannover
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Ontario
TORONTO
Molecular Diagnosis of Famialial Adenomatous Polyposis (APC sequencing and MLPA analysis)
Mount Sinai Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Technique(s)
: MLPA based techniques

Niedersachsen
GÖTTINGEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH 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
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

Nordrhein-Westfalen
KÖLN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Baden-Württemberg
TÜBINGEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Bayern
WÜRZBURG
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Universität Würzburg - Biozentrum
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

AUVERGNE-RHONE-ALPES
CLERMONT-FERRAND
Diagnosis of cancer predisposing syndrome (Panel)
CLCC Jean Perrin
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: NGS sequencing (except WES)

NORMANDIE
ROUEN
Diagnosis of susceptibility to colon cancer (polyposis and non-polyposis) (Panel)
Faculté de médecine et de pharmacie de Rouen
Purpose(s)
: Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

ILE-DE-FRANCE
PARIS
Diagnosis of familial adenomatous polyposis (Panel)
CLCC Institut Curie
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

ILE-DE-FRANCE
PARIS
Diagnosis of predisposition to colon-rectal tumors (Panel)
CLCC Institut Curie
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

HAUTS-DE-FRANCE
LILLE
Diagnosis of intestinal polyposis syndrome (Panel)
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s)
: Pre-symptomatic diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Methylation analysis, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques, BS-Pyrosequencing

BRETAGNE
RENNES
Diagnosis of predisposition to intestinal polyposis and digestive tract cancers (Panel)
CHU de Rennes - Hôpital Pontchaillou
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: NGS sequencing (except WES)

Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of hereditary breast, colon and ovarian cancer syndromes (gene panel)
Reference Laboratory Genetics
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Bayern
MÜNCHEN
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Medizinisch Genetisches Zentrum München
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Baden-Württemberg
ULM
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Ulm
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Bayern
WÜRZBURG
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universität Würzburg - Biozentrum
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Comunidad Valenciana
PATERNA
Diagnosis of familial adenomatous polyposis (APC gene)
Sistemas Genómicos S.L.
Purpose(s)
: Pre-implantation diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis
Technique(s)
: PCR based techniques

Merseyside
LIVERPOOL
Molecular diagnosis of Familial Adenomatous Polyposis - FAP (APC gene)
Liverpool Women's NHS Foundation Trust
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

West Yorkshire
LEEDS
Molecular diagnosis of Familial Adenomatous Polyposis (full coding region sequencing and dosage analysis, APC gene)
St James's University Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Bayern
BAD STEBEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Institut für angewandte Humangenetik und Onkogenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Tyne & Wear
NEWCASTLE UPON TYNE
Molecular diagnosis of Familial Adenomatous Polyposis (APC gene: Testing for known mutations in family members / Gene tracking)
Newcastle upon Tyne Hospitals NHS Trust
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis
Technique(s)
: Sanger sequencing

Antrim and Newtownabbey
BELFAST
Molecular diagnosis of Familial Adenomatous Polyposis by testing for known mutations in family members (APC1 gene)
Belfast City Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

WIEN
WIEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Medizinische Universität Wien
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Greater London
HARROW
Diagnosis of Familial adenomatous polyposis - FAP (APC gene: full gene mutation scan)
North West London Hospitals NHS - Northwick Park & St Marks Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), MLPA based techniques

AUVERGNE-RHONE-ALPES
LYON
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
CHU de Lyon HCL - GH Edouard Herriot
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
Technique(s)
: Sanger sequencing, PCR based techniques, MLPA based techniques

LAZIO
ROMA
Molecular diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Azienda Ospedaliera S. Camillo-Forlanini - Ospedale San Camillo
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

CAMPANIA
NAPOLI
Molecular diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Biotecnologie Avanzate Srl
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Bayern
ERLANGEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Humangenetisches Institut am Universitätsklinikum Erlangen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Galicia
SANTIAGO DE COMPOSTELA
Molecular diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
CHUS - Complejo Hospitalario Universitario de Santiago
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Cataluña
BARCELONA
Diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Centro de Diagnóstico Biomédico - CDB
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), MLPA based techniques

SUL
LISBOA
Molecular diagnosis of familial adenomatous polyposis (APC and MYH genes)
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Suisse Alémanique
BASEL
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Universitätsspital Basel
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Aragón
ZARAGOZA
Diagnosis of familial adenomatous polyposis (APC gene)
Hospital Universitario Miguel Servet
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

NORTE
PORTO
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Instituto Português de Oncologia do Porto, EPE / IPOFG - CRO Porto
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Nordrhein-Westfalen
BONN
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Universitätsklinikum Bonn
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

FRIULI VENEZIA GIULIA
AVIANO
Molecular diagnosis of familial adenomatous polyposis, autosomal recessive (MUTYH gene) and dominant (APC gene)
Centro di Riferimento Oncologico
Purpose(s)
: Post-natal diagnosis, Risk assessment
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), MLPA based techniques

LAZIO
ROMA
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Laboratorio Genoma
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Nordrhein-Westfalen
MÜNSTER
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Institut für Humangenetik des Universitätsklinikums Münster
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Niedersachsen
OSNABRÜCK
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Praxis Dres. Gencik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Sachsen
DRESDEN
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
BARCELONA
Diagnosis of the familial adenomatous polyposis (APC gene; SNP array)
Reprogenetics Spain S.A.
Purpose(s)
: Pre-implantation diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis
Technique(s)
: Sanger sequencing, PCR based techniques

Madrid
MADRID
Molecular diagnosis of intestinal polyposis syndrome (APC, MUTYH, SMAD4 genes)
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Hamburg
HAMBURG
Molecular diagnosis of familial adenomatous polyposis (APC gene: sequencing/ MLPA; MUTYH gene: sequencing)
Pränatalzentrum Hamburg und Humangenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Baden-Württemberg
STUTTGART
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes: sequencing, MLPA)
Praxis für Humangenetik und Prävention
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Andalucía
MÁLAGA
Diagnosis of familial adenomatous polyposis (APC gene; MUTYH gene / Y165C, G382D mutations)
Genetaq
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

Andalucía
ARMILLA
Molecular diagnosis of familial adenomatous polyposis (entire coding sequence of APC gene; MUTYH gene / mutations G382D and Y165C)
Lorgen G.P.
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region

Andalucía
SEVILLA
Diagnosis of familial adenomatous polyposis (APC gene)
Hospital Universitario Virgen del Rocío
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, PCR based techniques, MLPA based techniques

TOSCANA
PISA
Molecular diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

Comunidad Valenciana
PATERNA
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Sistemas Genómicos S.L.
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

LOMBARDIA
MONZA
Molecular diagnosis of familial adenomatous polyposis (APC, MUTYh genes)
Consorzio per la Genetica Molecolare Umana
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

País Vasco
SAN SEBASTIÁN
Diagnosis of familial adenomatous polyposis (APC gene, kit P043)
Hospital Universitario Donostia
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Deletion / Duplication analysis
Technique(s)
: MLPA based techniques

SUL
LISBOA
Molecular diagnosis of familial adenomatous polyposis (APC and MYH gene)
Faculdade de Medicina da Universidade de Lisboa
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Comunidad Valenciana
PATERNA
Molecular diagnosis of APC-related familial adenomatous polyposis (APC / MLPA, complete sequencing, detection of mutations p.Gln1062X and p.Glu1309AspfsX)
IMEGEN - Instituto de Medicina Genómica
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, Whole Exome Sequencing (WES)

Cataluña
L'HOSPITALET DE LLOBREGAT
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes - sequencing/MLPA)
Institut Català d'Oncologia
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Technique(s)
: MLPA based techniques

País Vasco
DERIO
Molecular diagnosis of familial adenomatous polyposis (aCGH)
Genetadi Biotech S.L.
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Sachsen
DRESDEN
Molecular diagnosis of familial adenomatous polyposis (APC, MSH3, MUTYH, NTHL1 genes)
Gemeinschaftspraxis für Humangenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

NORTE
PORTO
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes: sequencing of the entire coding region, deletion/duplication analysis by MLPA and analysis of targeted mutations Y165C and G382D)
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
Technique(s)
: MLPA based techniques

OCCITANIE
TOULOUSE
Molecular diagnosis of familial adenomatous polyposis (APC gene)
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
Technique(s)
: Sanger sequencing, MLPA based techniques

País Vasco
SAN SEBASTIÁN
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
Technique(s)
: Array based techniques

La Rioja
LOGROÑO
Diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Fundación Rioja Salud - Centro de Investigación Biomédica de La Rioja
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Cataluña
TERRASSA
Diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Consorci Sanitari de Terrassa
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), MLPA based techniques

Baden-Württemberg
STUTTGART
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Klinikum Stuttgart - Standort Olgahospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

ILHAS
FUNCHAL
Molecular diagnosis of familial adenomatous polyposis (APC gene: Sequencing of the exon 1-15)
Universidade da Madeira
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Cataluña
BARCELONA
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Hospital del Mar
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Cataluña
SABADELL
Diagnosis of familial adenomatous polyposis and attenuated (APC, MUTYH genes)
Corporación Sanitaria Parc Taulí
Purpose(s)
: Post-natal diagnosis, Risk assessment
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Mecklenburg-Vorpommern
GREIFSWALD
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH 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, Deletion / Duplication analysis
Technique(s)
: Sanger sequencing, MLPA based techniques

Hessen
WIESBADEN
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Institut für Humangenetik Wiesbaden
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

ILE-DE-FRANCE
PARIS
Predisposition to tumors (melanoma, pancreas, kidney, breast-ovary, colon, skin cancers) (Panel)
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Purpose(s)
: Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

GRAND-EST
STRASBOURG
Diagnosis of digestive tract tumor (Panel)
CHU de Strasbourg - Hôpital de Hautepierre
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

País Vasco
SAN SEBASTIÁN
Diagnosis of colon cancer (panel)
DNA Data
Purpose(s)
: Risk assessment
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Alberta
CALGARY
Pediatric Cancer NGS Panel (12 genes)
Alberta Children's Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), PCR based techniques, MLPA based techniques, Array based techniques

Alberta
CALGARY
Molecular Diagnosis of Familial Adenomatous Polyposis (NFLD mutation)
Alberta Children's Hospital
Purpose(s)
: Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis
Technique(s)
: Sanger sequencing

ILE-DE-FRANCE
PARIS
Diagnosis of familial adenomatous polyposis (Panel)
CHU Paris Centre - Hôpital Cochin
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: NGS sequencing (except WES)

Sachsen
DRESDEN
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

VENETO
COSTOZZA DI LONGARE
Molecular diagnosis of Gardner syndrome (APC gene)
B.I.R.D. Foundation
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic 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
Technique(s)
: Sanger sequencing

Baden-Württemberg
FREIBURG
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Institut für Humangenetik am Universitätsklinikum Freiburg
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
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

OCCITANIE
MONTPELLIER
Diagnosis of predisposition to colorectal cancer (Panel)
CHRU de Montpellier - Hôpital Arnaud de Villeneuve
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

ILE-DE-FRANCE
VILLEJUIF
Diagnosis of tumors (Panel)
CLCC Institut Gustave Roussy
Purpose(s)
: Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: NGS sequencing (except WES)

GRAND-EST
VANDOEUVRE-LÈS-NANCY
Diagnosis of predisposition to breast, ovarian and colon cancer (Panel)
CHU de Nancy - Hôpitaux de Brabois
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

WIEN
WIEN
Molecular diagnosis of (attenuated) familial adenomatous polyposis (APC, AXIN2, MSH3, and MUTYH genes)
Praxis für Humangenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
REUS
Diagnosis of the familial adenomatous polyposis (MUTYH and APC genes)
Hospital Universitari de Sant Joan de Reus
Purpose(s)
: Pre-symptomatic diagnosis, Risk assessment
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

WIEN
WIEN
Molecular diagnosis of Gardner syndrome (APC gene)
Medizinische Universität Wien
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
ESPLUGUES DE LLOBREGAT
Diagnosis of colorectal cancer (panel, qCancer CCR)
qGenomics
Purpose(s)
: Risk assessment
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

VENETO
PADOVA
Molecular diagnosis of hereditary liver diseases [panel of genes]
Research&Innovation S.r.l. (R&I Genetics)
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
Technique(s)
: NGS sequencing (except WES), Whole Exome Sequencing (WES)

PUGLIA
CASTELLANA GROTTE
Molecular diagnosis od familial adenomatous polyposis (APC, MYH genes)
IRCCS "Saverio De Bellis"
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

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

Sachsen-Anhalt
HALLE (SAALE)
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

PIEMONTE
CANDIOLO
Molecular diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Istituto per la Ricerca e la Cura del Cancro
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Madrid
MADRID
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Centro Nacional de Investigaciones Oncológicas (CNIO)
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Jylland
AARHUS
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH gene sequencing and MLPA)
Aarhus Universitetshospital - Skejby
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Technique(s)
: MLPA based techniques

LOMBARDIA
MILANO
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Ospedale Niguarda Ca' Granda
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Cyprus
NICOSIA
Mutation screening of familial adenomatous polyposis (APC 5q22.2)
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

ATTIKI
ATHENS
Molecular diagnosis of familial adenomatous polyposis (APC gene)
BIOGENOMICA
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

LIGURIA
GENOVA
Molecular diagnosis of familial adenomatous polyposis, autosomal recessive and dominant
Istituto Nazionale per la Ricerca sul Cancro - IST
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Mecklenburg-Vorpommern
ROSTOCK
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes)
Albrecht-Kossel-Institute for Neuroregeneration (AKos)
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Capital City Prague
PRAHA
Prenatal and postnatal molecular diagnosis of familial autosomal dominant adenomatous polyposis (APC gene)
First Faculty of Medicine and General Teaching Hospital
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Fyn
ODENSE
Molecular diagnosis of familial adenomatous polyposis (APC gene sequencing)
Amplexa Genetics A/S
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

PUGLIA
SAN GIOVANNI ROTONDO
Molecular diagnosis of familial adenomatous polyposis (APC gene)
IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

ISRAEL
RAMAT GAN
Molecular diagnosis of Colon cancer (APC, MSH2, Mutation analysis, PGD)
Sheba Medical Center
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

ISRAEL
PETAH TIKVA
Molecular diagnosis of familial adenomatous polyposis (APC, Mutation analysis)
Rabin Medical Center - Beilinson Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Capital City Prague
PRAHA
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Charles University - First faculty of medicine
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

ATTIKI
ATHENS
Molecular diagnosis of familial adenomatous polyposis (APC and MUTYH genes: full sequencing)
National center for scientific research Demokritos
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

ISRAEL
TEL AVIV
Molecular diagnosis of familial adenomatous polyposis (APC full gene sequencing)
Pronto Diagnostics Ltd.
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

BUCURESTI
BUCURESTI
Postnatal molecular diagnosis of familial adenomatous polyposis (APC gene:deletion/duplication analysis by MLPA)
National institute of legal medicine
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Deletion / Duplication analysis
Technique(s)
: MLPA based techniques

Madrid
SAN SEBASTIÁN DE LOS REYES
Diagnosis of familial adenomatous polyposis (APC gene / deletions in exon 15; MUTYH gene)
Laboratorio de Genética Clínica, S.L.
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic 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
Technique(s)
: Sanger sequencing, MLPA based techniques

Madrid
MAJADAHONDA
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Genyca Innova
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

SARDEGNA
CAGLIARI
Molecular diagnosis of familial adenomatous polyposis (APC, MUTYH genes)
Ospedale "R. Binaghi"
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Berlin
BERLIN
Molecular diagnosis of cancer (NGS Cancer Panel)
ATG GenMed GmbH
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Québec
MONTRÉAL
Molecular diagnosis of familial adenomatous polyposis (APC gene by MLPA, Mutation I1307K, unknown mutation by PTT, individual mutation by sequencing & PTT)
Hôpital général juif - Jewish General Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis
Technique(s)
: MLPA based techniques

PUGLIA
LECCE
Molecular diagnosis of familial adenomatous polyposis (APC gene)
Presidio Ospedaliero "Vito Fazzi" - ASL LE
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Cyprus
NICOSIA
Analysis for known mutations of familial adenomatous polyposis (APC 5q22.2)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

BOURGOGNE-FRANCHE-COMTE
DIJON