Funded by the
National Institutes of Health

L1 Syndrome | L1 Disease | L1 Spectrum
Includes: MASA Syndrome | Spastic Paraplegia 1 | X-Linked Corpus Callosum Agenesis | X-Linked Hydrocephalus with Stenosis of the Aqueduct of Sylvius

Select all clinical laboratories
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Analysis of the entire coding region: Mutation scanning	Deletion/duplication analysis	Prenatal diagnosis	Carrier testing
Centogene GmbH Institute of Molecular Diagnostics Rostock, Germany Christoph Ehlers
Edith Wolfson Medical Center Molecular Genetics Laboratory Holon, Israel Esther Leshinsky-Silver, PhD
GeneDx Gaithersburg, MD Sherri J Bale, PhD, FACMG; John G Compton, PhD; Anne Maddalena, PhD, FACMG ; Gabriele Richard, MD, FACMG
Greenwood Genetic Center Molecular Diagnostic Laboratory Greenwood, SC Julie Jones, PhD; Monica Basehore, PhD
St Mary's Hospital Manchester Regional Molecular Genetics Service Manchester, United Kingdom Rob Elles, Dr, PhD, FRCPath; Andrew Wallace, Dr, PhD, DipRCPath
University Medical Center Groningen DNA Diagnostics Laboratory Groningen, Netherlands Cisca Wijmenga, PhD

Copyright© 1993-2009,
All Rights Reserved
University of Washington, Seattle
Terms of Use

Funding Support
National Library of Medicine, NIH
National Human Genome Research Institute, NIH

Sponsoring Institution
University of Washington
Seattle, Washington