Funded by the
National Institutes of Health

Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome | HHH Sydrome

Select all clinical laboratories
Laboratories offering clinical testing:	Targeted mutation analysis	Analyte	Enzyme assay	Prenatal diagnosis	Carrier testing
ARUP Laboratories Biochemical Genetics Laboratory Salt Lake City, UT Edward R Ashwood, MD; Marzia Pasquali, PhD; Nicola Longo, MD, PhD; Patrice Held, 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
Baylor Research Institute Institute of Metabolic Disease Dallas, TX Charles R Roe, MD; Lawrence Sweetman, PhD; Xiaowei Fu, PhD, MD; Teodoro Bottiglieri, PhD; Jiahuan Ding, MD, PhD; Bingzhi Yang, MD; Raphael Schiffmann, MD
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
Hospital Sainte-Justine Biologie Moleculaire Montreal, Quebec, Canada Georges-Etienne Rivard, MD; Li Fan, MD, PhD, FCCMG
Massachusetts General Hospital Amino Acid Disorder (Neurochemistry) Lab Charlestown, MA Vivian E Shih, MD
Oregon Health & Science University Biochemical Genetics Laboratory/ Portland, OR Cary O Harding, MD, FACMG; Sue Richards, PhD
PerkinElmer Genetics, Inc. Bridgeville, PA Joseph M Quashnock, PhD, HCLD(ABB), FACB; Zhili Lin, MD, PhD, HCLD(ABB), FACB; John E Sherwin, PhD, DABCC
University of Alabama at Birmingham UAB Biochemical Genetics Laboratory Birmingham J Daniel Sharer, PhD, FACMG; S Lane Rutledge, MD, FACMG
University of California San Diego UCSD Biochemical Genetics Laboratory La Jolla, CA Bruce A Barshop, MD, PhD; William L Nyhan, MD, PhD
University of Colorado and Health Sciences Center UCDHSC Biochemical Genetics Laboratory Aurora, CO Stephen I Goodman, MD; Michael Woontner, PhD

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

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