Funded by the
National Institutes of Health

Saethre-Chotzen Syndrome | Acrocephalosyndactyly Type III
Includes: Robinow-Sorauf Syndrome

Select all clinical laboratories
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Analysis of the entire coding region: Mutation scanning	FISH-metaphase	FISH-interphase	Deletion/duplication analysis	Prenatal diagnosis
Center for Genetic Testing at Saint Francis Genetics Laboratory Tulsa, OK Nancy J Carpenter, PhD, FACMG; Frederick V Schaefer, PhD, FACMG; Michael A Kayser, DO, FACMG
Children's Hospital of Philadelphia Molecular Genetics Laboratory Philadelphia, PA Catherine A Stolle, PhD; Avni Santani, PhD
Greenwood Genetic Center Molecular Diagnostic Laboratory Greenwood, SC Julie Jones, PhD; Monica Basehore, PhD
Johns Hopkins Hospital DNA Diagnostic Laboratory Baltimore, MD Garry R Cutting, MD; Steven J Steinberg, PhD
Oxford Medical Genetics Laboratories Oxford Genetics Laboratories Oxford, Oxon, United Kingdom Anneke Seller, BSc(Hons), PhD, (MRCPath)
Signature Genomic Laboratories Spokane, WA Lisa G Shaffer, PhD, FACMG; Bassem A Bejjani, MD, FACMG; Beth Torchia, PhD, FACMG; Roger Schultz, PhD; Allen Lamb, PhD
The Hospital for Sick Children Molecular Genetics Laboratory Toronto, Ontario, Canada Peter N Ray, PhD, FCCMG, FACMG; Tracy L Stockley, PhD, FCCMG
University of Nebraska Medical Center Human Genetics Laboratory, Munroe-Meyer Institute Omaha, NE Warren G Sanger, PhD, FACMG; Bhavana J Dave, PhD, FACMG

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National Human Genome Research Institute, NIH

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