Laboratory	Test Method	Prenatal	Carrier *
Asper Biotech Ltd., Asper Biotech - Tartu, Estonia	• Sequence analysis of the entire coding region • Targeted mutation analysis
ATS GeneTech Private Limited, GeneTech - Hyderabad, India	• Sequence analysis of select exons
bio.logis Center for Human Genetics - Frankfurt, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Biyolojik Bilimler Arastirma Gelistirme ve Uretim AS, Duzen Laboratuvarlar Grubu - Istanbul, Turkey	• Sequence analysis of the entire coding region
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany	• Sequence analysis of the entire coding region
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Center for Human Genetics, Inc - Cambridge, MA, USA	• Targeted mutation analysis
Centogene AG, Rare Disease Company - Rostock, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
CGC Genetics - Porto, Portugal	• Sequence analysis of the entire coding region
Children's Hospital of Eastern Ontario, Molecular Genetics Diagnostic Laboratory - Ottawa, Canada	• Sequence analysis of the entire coding region • Targeted mutation analysis • Deletion/duplication analysis
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel	• Targeted mutation analysis
GENDA - Ciudad autonoma de Buenos Aires, Argentina	• Targeted mutation analysis
GENETAQ, Molecular Genetics Centre - Malaga, Spain	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Genetic Diagnosis and Research Center, Genetiks - Istanbul, Turkey	• Sequence analysis of the entire coding region
GENETIX Centro de Investigación en Genética Humana y Reproductiva - Bogota, Colombia	• Sequence analysis of the entire coding region • Sequence analysis of select exons
GENNET s.r.o., Laboratory of Molecular Genetics - Prague, Czech Republic	• Mutation scanning of the entire coding region • Deletion/duplication analysis
GGA - Galil Genetic Analysis - Kazerin, Israel	• Sequence analysis of the entire coding region
GSTS Pathology, DNA Laboratory - London, Great Britain	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Health Care Center GENOMED, Laboratory of Human Genetics - Warsaw, Poland	• Sequence analysis of the entire coding region
HUSLAB, Laboratory of Genetics - Helsinki, Finland	• Targeted mutation analysis
Innovagenomics S.L, Innovagenomics - Salamanca, Spain	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Institut de Cancrologie Gustave Roussy, Laboratoire de Gntique - Villejuif, France	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Institute of Medical Genetics, All Wales Molecular Genetics Laboratory - Cardiff, Great Britain	• Sequence analysis of the entire coding region • Targeted mutation analysis • Deletion/duplication analysis
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain	• Sequence analysis of the entire coding region • Sequence analysis of select exons • Deletion/duplication analysis
Instituto de Referencia Andino, Unidad de Diagnostico Molecular - Bogotá, Colombia	• Targeted mutation analysis
Kingston General Hospital, Molecular Diagnostic Laboratory - Kingston, Canada	• Mutation scanning of the entire coding region
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
LabPLUS - Auckland City Hospital, Molecular Genetics Laboratory - Diagnostics Genetics - Auckland, New Zealand	• Sequence analysis of the entire coding region • Deletion/duplication analysis
London Health Sciences Centre, Molecular Diagnostic Laboratory - London, Canada	• Sequence analysis of the entire coding region • Targeted mutation analysis • Deletion/duplication analysis
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands	• Sequence analysis of the entire coding region
Masaryk Memorial Cancer Institute, Cancer Epidemiology and Genetics - Brno, Czech Republic	• Sequence analysis of the entire coding region • Mutation scanning of the entire coding region
Medgene, MedGene - Bratislava, Slovakia	• Sequence analysis of the entire coding region
MGZ München, Medizinisch Genetisches Zentrum Mnchen - München, Germany	• Mutation scanning of the entire coding region • Deletion/duplication analysis
Mount Sinai Hospital, Advanced Molecular Diagnostics - Toronto, Canada	• Sequence analysis of the entire coding region • Targeted mutation analysis • Deletion/duplication analysis
Myriad Genetic Laboratories, Inc., Myriad Genetic Laboratories - Salt Lake City, UT, USA	• Sequence analysis of the entire coding region • Targeted mutation analysis • Deletion/duplication analysis
North York General Hospital, Molecular Genetics Laboratory - Toronto, Canada	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain	• Sequence analysis of the entire coding region • Targeted mutation analysis • Deletion/duplication analysis
Peter MacCallum Cancer Centre, Molecular Diagnostic Pathology - Melbourne, Australia	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Praxis fuer Humangenetik Wien - Vienna, Austria	• Sequence analysis of the entire coding region
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA	• Deletion/duplication analysis
Pronto Diagnostics Ltd., ProntoLab - MLPA Lab - Tel Aviv, Israel	• Sequence analysis of the entire coding region • Targeted mutation analysis • Deletion/duplication analysis
Rabin Medical Center, Molecular Genetics - Petah Tikva, Israel	• Targeted mutation analysis
Samsung Medical Center, Department of Laboratory Medicine and Genetics - Seoul, South Korea	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Seoul National University Hospital, Molecular Diagnostics Laboratory - Seoul, South Korea	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Shaare Zedek Medical Center, Medical Genetics Institute - Jerusalem, Israel	• Targeted mutation analysis • Linkage analysis
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain	• Sequence analysis of the entire coding region • Deletion/duplication analysis
St George's University of London, SW Thames Molecular Genetics Diagnostic Laboratory - London, UK, Great Britain	• Sequence analysis of the entire coding region • Deletion/duplication analysis
St James's University Hospital, Leeds Teaching Hospitals, Yorkshire Regional DNA Laboratory - Leeds, Great Britain	• Sequence analysis of the entire coding region • Deletion/duplication analysis
St. Elisabeth Cancer Institute, Department of Clinical Genetics - Heydukova 2, Slovakia	• Sequence analysis of the entire coding region
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
University Hospital of Tuebingen, Medical Genetics Tuebingen - Tuebingen, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
University of California Los Angeles, UCLA Diagnostic Molecular Pathology Laboratory - Los Angeles, CA, USA	• Sequence analysis of select exons • Targeted mutation analysis
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA	• Targeted mutation analysis
University of Goettingen, Institute of Human Genetics - Goettingen, Germany	• Sequence analysis of the entire coding region • Deletion/duplication analysis
University of North Carolina Hospitals, Molecular Genetics - Chapel Hill, NC, USA	• Mutation scanning of the entire coding region • Targeted mutation analysis

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.