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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations

S Nimkarn1, B I Cerame, J Q Wei

  • 1Department of Pediatrics, Weill Medical College of Cornell University, New York, New York 10021, USA.

The Journal of Clinical Endocrinology and Metabolism
|January 27, 1999
PubMed

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