Funded by the
National Institutes of Health

FGFR2-Related Craniosynostosis
Includes: Apert Syndrome | Beare-Stevenson Syndrome | Crouzon Syndrome | FGFR2-Related Isolated Coronal Synostosis | Jackson-Weiss Syndrome | Pfeiffer Syndrome Type 1, 2 and 3

Select all clinical laboratories
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Sequence analysis of select exons	Targeted mutation analysis	Linkage analysis	Mutation scanning of select exons	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
Center for Human Genetics Bioscientia GmbH Ingelheim, Germany Jochen Decker, MD, PhD
Children's Hospital Boston DNA Diagnostic Laboratory Boston, MA Bai-Lin Wu, PhD, FACMG; David T Miller, MD, PhD, FACMG; Yiping Shen, PhD, FACMG
Children's Hospital of Philadelphia Molecular Genetics Laboratory Philadelphia, PA Catherine A Stolle, PhD; Avni Santani, PhD
Children's Mercy Hospital and Clinics Children's Mercy Hospital Molecular Genetics Laboratory Kansas City, MO Carol Saunders, PhD
Comprehensive Genetic Services, SC Molecular Diagnostic Laboratory Milwaukee, WI Anthony T Garber, PhD; Christine R Bryke, MD, FABMG
Greenwood Genetic Center Molecular Diagnostic Laboratory Greenwood, SC Julie Jones, PhD; Monica Basehore, PhD
Hospital Sainte-Justine Biologie Moleculaire Montreal, Quebec, Canada Georges-Etienne Rivard, MD; Li Fan, MD, PhD, FCCMG
Johns Hopkins Hospital DNA Diagnostic Laboratory Baltimore, MD Garry R Cutting, MD; Steven J Steinberg, PhD
Motol University Hospital Medical Molecular Genetics Prague, Czech Republic Milan Macek, Jr, Prof, MD, PhD
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Sequence analysis of select exons	Targeted mutation analysis	Linkage analysis	Mutation scanning of select exons	Prenatal diagnosis
Oxford Medical Genetics Laboratories Oxford Genetics Laboratories Oxford, Oxon, United Kingdom Anneke Seller, BSc(Hons), PhD, (MRCPath)
Sir Ganga Ram Hospital Department of Genetic Medicine New Delhi, India I C Verma, MD, FAAP, FRCP, FAMS; Renu Saxena, PhD; Meena Lall, PhD
Sistemas Genomicos Medical Genetics Unit Paterna, Valencia, Spain Javier Garcia-Planells, PhD
Stanford Clinical Laboratories Molecular Pathology Laboratory Palo Alto, CA Iris Schrijver, MD; James L Zehnder, MD
The Hospital for Sick Children Molecular Genetics Laboratory Toronto, Ontario, Canada Peter N Ray, PhD, FCCMG, FACMG; Tracy L Stockley, PhD, FCCMG
University of Calgary Molecular Diagnostic Laboratory Calgary, Alberta, Canada Peter Bridge, PhD, FCCMG, FACMG; Jillian Parboosingh, PhD, FCCMG

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

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University of Washington
Seattle, Washington