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National Institutes of Health

CHILD Syndrome | Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects

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Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Analyte	Enzyme assay	Prenatal diagnosis	Carrier testing
Academic Medical Centre, University of Amsterdam Laboratory Genetic Metabolic Diseases Amsterdam, Netherlands Ronald JA Wanders, PhD
Kennedy Krieger Institute Biochemical Genetics Laboratory Baltimore, MD Richard I Kelley, MD, PhD; Lisa E. Kratz, PhD
University of Chicago University of Chicago Genetic Services Chicago, IL Soma Das, PhD; Stuart Schwartz, PhD, FACMG

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National Human Genome Research Institute, NIH

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