Funded by the
National Institutes of Health

Mucopolysaccharidosis Type I | Alpha-L-Iduronidase Deficiency | IDUA Deficiency | MPS I
Includes: Hurler Syndrome | Hurler-Scheie Syndrome | Scheie Syndrome

Select all clinical laboratories
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Targeted mutation analysis	Analyte	Enzyme assay	Deletion/duplication analysis	Prenatal diagnosis	Carrier testing
A Zebraic® Corporation Minneapolis, MN Chester B Whitley, PhD, MD
Adelaide Women's and Children's Hospital National Referral Laboratory North Adelaide, Australia Michael J Fietz, PhD
Baylor College of Medicine Medical Genetics Laboratories Houston, TX Christine M Eng, MD, FACMG; William E O'Brien, PhD; Lee-Jun Wong, PhD; Sau W. Cheung, PhD
Centogene GmbH Institute of Molecular Diagnostics Rostock, Germany Christoph Ehlers
Centre for DNA Fingerprinting and Diagnostics Diagnostics Division Hyderabad, India Ashwin B Dalal, DM (Medical Genetics)
Charles University, 1st Faculty of Medicine Institute of Inherited Metabolic Disorders Praha, Czech Republic Milan Elleder, MD, PhD
Children's Hospital and Regional Medical Center Biochemical and Molecular Genetics Laboratories Seattle, WA Sihoun Hahn, MD, PhD; Rhona Jack, PhD; C Ronald Scott, MD
Emory University School of Medicine Emory Biochemical Genetics Laboratory Atlanta, GA Fran Kendall, MD; Miao He, PhD
Emory University School of Medicine Emory Molecular Genetics Laboratory Atlanta, GA Madhuri Hegde, PhD, FACMG; Bradford Coffee, PhD, FACMG; Lora JH Bean, PhD, FACMG
Greenwood Genetic Center Metabolic Laboratory Greenwood, SC Tim C Wood, PhD
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Targeted mutation analysis	Analyte	Enzyme assay	Deletion/duplication analysis	Prenatal diagnosis	Carrier testing
Mayo Clinic - Minnesota Biochemical Genetics Laboratory Rochester, MN Dietrich Matern, MD; Piero Rinaldo, MD, PhD; Silvia Tortorelli, MD, PhD; Dimitar K Gavrilov , MD, PhD; Devin Oglesbee, PhD; Kimiyo Raymond, MD
New York State Institute for Basic Research in Developmental Disabilities Biochemical Genetics Staten Island, NY Milen Velinov, MD, PhD
New York University School of Medicine NYU Neurogenetics Laboratory New York, NY Edwin H Kolodny, MD
Oregon Health & Science University Biochemical Genetics Laboratory/ Portland, OR Cary O Harding, MD, FACMG; Sue Richards, PhD
Thomas Jefferson University Lysosomal Diseases Testing Laboratory Philadelphia, PA David A Wenger, PhD; Paola Luzi, PhD
University of Alabama at Birmingham Metabolic Disease Laboratory Birmingham Jerry N Thompson, PhD, FACMG
University of Colorado and Health Sciences Center UCDHSC Biochemical Genetics Laboratory Aurora, CO Stephen I Goodman, MD; Michael Woontner, PhD
University of Illinois Medical Center at Chicago Biochemical Genetics Laboratory Chicago, IL George Hoganson, MD
University of Maryland Pediatric Biochemical Genetics Laboratory Baltimore, MD Erin T Strovel, PhD; Miriam G Blitzer, PhD
University of Minnesota Medical School Gene Therapy and Diagnostics Lab Minneapolis, MN Chester B Whitley, PhD, MD

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

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University of Washington
Seattle, Washington