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Caption : Accreditation =Accreditation
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    • FRANCE
    • HAUTE-NORMANDIE
    • BOIS-GUILLAUME
    • Accreditation
    • Cytogenetic diagnosis of Fanconi anemia (by searching chromosomal breakpoints)
    • Etablissement français du sang - Normandie
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Ashkenazes carrier screening (ASHPLEX 1, ASHPLEX 2, ASHPLEX Gaucher)
    • Centre Médical Universitaire - CMU
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCC, FANCG, FANCE, FANCF genes)
    • Charité - Universitätsmedizin Berlin (CVK)
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Ashkenazes carrier screening (ASHPLEX 1, ASHPLEX 2, ASHPLEX Gaucher)
    • Genetica AG
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Fanconi Anaemia (FANCA, FANCC & FANCG: sequencing of coding regions; dosage analysis of FANCA)
    • Sheffield Children's NHS Foundation Trust
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCC, FANCG genes)
    • Universität Würzburg - Biozentrum
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Cytogenetic diagnosis of Fanconi Anaemia (by chromosome breakage analysis)
    • Birmingham Women's NHS Foundation Trust
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (BRIP1, PALB2 genes)
    • Zentrum für Humangenetik Mannheim
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by CGH arrays
    • Universität Zürich
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (BRIP1, BRCA2, FANCA, FANCB, FANCC, FANCD2,FANCF, FANCG, FANCL, PALB2, ERCC4, FANCI, RAD51C, SLX4, FAN1 and FANCM genes)
    • Universität Zürich
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Fanconi Anemia (BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCL, FANCM and FANCI gene)
    • VUmc - VU medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCC genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Cytogenetic diagnosis of Fanconi Anaemia (by chromosome breakage analysis)
    • Southmead Hospital
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Cytogenetic diagnosis of Fanconi Anaemia (by chromosome breakage studies)
    • University Hospital of Wales
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular screening of frequent diseases in Ashkenazi Jewish populations (APEX: ABCC8, AGL, ASPA, BCKDHB, BLM, CFTR, CLRN1, DLD, F11, FANCC, G6PC, GBA, GJB2, HEXA, IKBKAP, LDLR, MCOLN1, MEFV, NEB, PCDH15, SERPINA1, SMPD1, TMEM216 and TOR1A genes)
    • Asper Biotech Ltd.
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM, FANCN genes)
    • Centogene AG
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (BRIP1, BRCA2, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2 genes)
    • MVZ Fenner & Krasemann
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • AARGAU
    • Accreditation
    • Molecular diagnosis of RAD51C related diseases (RAD51C gene: sequencing and deletion analysis)
    • Kantonsspital Aargau
    • More information
    • UNITED KINGDOM
    • Grampian
    • ABERDEEN
    • Accreditation
    • Cytogenetic diagnosis of Fanconi Anaemia (by chromosome breakage analysis)
    • Aberdeen Royal Infirmary, Polwarth Building
    • More information
    • CANADA
    • Ontario
    • TORONTO
    • Accreditation
    • Molecular Diagnosis of Fanconi Anemia type C (FANCC targeted mutation analysis)
    • The Hospital for Sick Children and University of Toronto
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCC, FANCG, PALB2 genes)
    • Reference Laboratory Genetics
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Fanconi Anemia, Complementation Group A (FANCA gene: Targetted mutation analysis)
    • Guy's Hospital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Fanconi Anemia, Complementation Group C (FANCC gene: Targetted mutation analysis / Testing for known mutations in family members)
    • Guy's Hospital
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Accreditation
    • Preimplantation genetic diagnosis of Fanconi anemia (FANCA gene)
    • Sistemas Genómicos S.L.
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of Fanconi anemia (PALB2 gene)
    • CeGaT GmbH
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Cytogenetic diagnosis of Fanconi Anaemia (by searching chromosomal breakpoints)
    • CHU de Lyon HCL - GH Est
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of Fanconi anemia (BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCI, FANCL, FANCM, FANCD2, FANCE, FANCF, FANCG, PALB2, RAD51C, SLX4 genes)
    • CLCC Institut Curie
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Fanconi anaemia (FANCC gene)
    • Laboratorio Genoma
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Cytogenetic diagnosis of Fanconi anemia
    • CIC - Centro de Investigación del Cáncer
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Molecular cytogenetic test for Fanconi anemia
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Cytogenetic diagnosis of Fanconi anemia (DEB-induced chromosome breakage)
    • Instituto de Ciências Biomédicas Abel Salazar
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Fanconi anemia (FANCA gene)
    • Sistemas Genómicos S.L.
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Molecular diagnosis of Fanconi anemia (BRCA2, BRIP1, PALB2, and RAD51C genes)
    • Medizinische Universität Graz
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of Fanconi anemia (BRCA2, FANCC genes)
    • Klinikum Stuttgart - Standort Olgahospital
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Cytogenetic diagnosis of Fanconi anemia
    • Diagnostic Genetic Center
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Fanconi anemia (FANCA gene: Sequencing of the entire coding region and deletion/duplication analysis by MLPA)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Fanconi anemia (NGS panel for BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, RAD51C genes: Sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • ITALY
    • LOMBARDIA
    • BUSTO ARSIZIO
    • Cytogenetic diagnosis of Fanconi anemia
    • Toma Advanced Biomedical Assays S.p.A.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of Fanconi anemia (FANCA gene / sequencing, MLPA; FANCC gene / gene and mutations sequencing; FANCG, PALB2 genes / sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Molecular cytogenetic diagnosis of Fanconi Anaemia (by conventional karyotype and FISH analysis)
    • Hammersmith Hospital
    • More information
    • SERBIA
    • Serbia
    • BELGRADE
    • Cytogenetic diagnosis of Fanconi anemia (diepoxybutane tests for chromosomal breakage)
    • Mother and Child Health Institute of Serbia "Dr Vukan Cupic"
    • More information
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Cytogenetic diagnosis of Fanconi Anaemia
    • The Churchill Hospital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • NETHERLANDS
    • Groningen
    • GRONINGEN
    • Cytogenetic diagnosis of Fanconi anemia
    • UMCG - Universitair Medisch Centrum Groningen
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCB, FANCC, FANCG genes)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • CANADA
    • Manitoba
    • WINNIPEG
    • Ashkenazi Jewish Panel (targeted mutation analysis of ASPA, FANCC, HEXA, IKBAP)
    • Health Sciences Centre
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Cytogenetics diagnosis of Fanconi anemia
    • Azienda Ospedaliero Universitaria "Policlinico Vittorio Emanuele"
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of Fanconi anemia (FANCA gene)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • ITALY
    • UMBRIA
    • PERUGIA
    • Cytogenetic and molecular cytogenetic diagnosis of Fanconi anaemia
    • Università degli Studi di Perugia - Ospedale S. Maria della Misericordia
    • More information
    • ITALY
    • LOMBARDIA
    • PAVIA
    • Cytogenetic diagnosis of Fanconi anemia
    • Fondazione IRCCS Policlinico San Matteo
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular cytogenetics diagnosis of Fanconi anemia
    • P.S.I. "Elena d'Aosta"
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Fanconi anemia (BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG and FANCI genes)
    • CIEMAT - Centro de Investigaciones Energéticas Medioambientales y Tecnológicas
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCC, FANCE, FANCF and FANCG genes / retrovirus-mediated identification of complementation groups)
    • CIEMAT - Centro de Investigaciones Energéticas Medioambientales y Tecnológicas
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Molecular diagnosis of Fanconi Anemia (FANCA gene)
    • Ospedale Regionale per le Microcitemie
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • UDINE
    • Cytogenetic diagnosis of Fanconi anemia
    • Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Prenatal and postnatal molecular diagnosis of Fanconi anemia (FANCA, FANCC genes)
    • Acibadem healthcare group
    • More information
    • ISRAEL
    • ISRAEL
    • BEER YAAKOV
    • Molecular diagnosis of Fanconi Anemia A (FANCA, Mutation analysis, Carrier screening)
    • Assaf Harofeh Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • BEER YAAKOV
    • Molecular diagnosis of Fanconi Anemia C (FANCC, Mutation analysis, Carrier screening)
    • Assaf Harofeh Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Fanconi anemia type A (FANCA, Mutation analysis, Carrier screening, PGD)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Fanconi Anemia type C (FANCC, Mutation analysis, Carrier screening, PGD)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Molecular diagnosis of Fanconi Anemia A (FANCA, Mutation analysis, Carrier screening)
    • Carmel Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Molecular diagnosis of Fanconi Anemia C (FANCC, Mutation analysis, Carrier screening)
    • Carmel Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • PETAH TIKVA
    • Molecular diagnosis of Fanconi Anemia A (FANCA, Mutation analysis, Carrier screening)
    • Rabin Medical Center - Beilinson Hospital
    • More information
    • ISRAEL
    • ISRAEL
    • PETAH TIKVA
    • Molecular diagnosis of Fanconi Anemia C (FANCC, Mutation analysis, Carrier screening)
    • Rabin Medical Center - Beilinson Hospital
    • More information
    • ISRAEL
    • ISRAEL
    • RAMAT-GAN
    • Molecular diagnosis of Fanconi anemia type A (FANCA, Mutation analysis, Carrier screening)
    • Sheba Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • RAMAT-GAN
    • Molecular diagnosis of Fanconi Anemia type C (FANCC, Mutation analysis, Carrier screening)
    • Sheba Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Molecular diagnosis of Fanconi anemia type A (FANCA, Mutation analysis, Carrier screening)
    • The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Molecular diagnosis of Fanconi Anemia type C (FANCC, Mutation analysis, Carrier screening)
    • The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
    • More information
    • ISRAEL
    • ISRAEL
    • REHOVOT
    • Molecular diagnosis of Fanconi anemia type A (FACA, Mutation analysis, Carrier screening)
    • Kaplan Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • REHOVOT
    • Molecular diagnosis of Fanconi Anemia type C (FAC C, Mutation analysis, Carrier screening)
    • Kaplan Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HOLON
    • Molecular diagnosis of Fanconi Anemia C (FANCC, Mutation analysis, Carrier screening, PGD)
    • Wolfson Medical Center
    • More information
    • SPAIN
    • Cataluña
    • BELLATERRA
    • Molecular diagnosis of Fanconi anemia (15 genes)
    • Universitat Autònoma de Barcelona. Facultat de Medicina
    • More information
    • SPAIN
    • Cataluña
    • BELLATERRA
    • Molecular diagnosis of Fanconi anemia (recurrent mutations of FANCA gene)
    • Universitat Autònoma de Barcelona. Facultat de Medicina
    • More information
    • ISRAEL
    • ISRAEL
    • PETAH TIKVA
    • Molecular diagnosis of Fanconi anemia (FANCD2, FANCA, FANCG, FANCC, FANCJ, FANCN and BRCA2 mutation analysis and MLPA)
    • Schneider Children Medical Centre of Israel
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Fanconi anemia (FANCA, FANCC, FANCG and PALB2 genes: entire coding sequence)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Preimplantation genetic diagnosis of Fanconi anemia (FANCE gene)
    • Igenomix Spain
    • More information
    • CANADA
    • Québec
    • QUÉBEC
    • Cytogenetic diagnosis of chromosomal breakage syndromes
    • CHUQ - Hôpital Saint-Francois d'Assise
    • More information
    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • Ashkenazi Jewish Carrier Screening (Founder Mutations in HEXA, IKBKAP, ASPA, FANCC)
    • BC Women's Hospital and Health Centre
    • More information