Funded by the
National Institutes of Health

Autoimmune Polyendocrinopathy Syndrome Type 1 | APS1 | Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy

Select all clinical laboratories
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Targeted mutation analysis	Deletion/duplication analysis	Prenatal diagnosis	Carrier testing
Amplexa Genetics A/S Amplexa Genetics Odense, Denmark Klaus Brusgaard, PhD, MSC; Hans Atli Dahl
Athena Diagnostics Inc Reference Lab Worcester, MA Sat Dev Batish, PhD, FACMG; Masamichi Ito, PhD, FACMG; Christine M Stanley, PhD, FACMG
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
Correlagen Diagnostics, Inc. Waltham, MA David T Miller, MD, PhD, FACMG
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
HUSLAB Laboratory of Molecular Genetics Helsinki, Finland Aarno Palotie, MD, PhD; Arto K Orpana, PhD
Oxford Medical Genetics Laboratories Oxford Genetics Laboratories Oxford, Oxon, United Kingdom Anneke Seller, BSc(Hons), PhD, (MRCPath)

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