Search All UT System Experts

Molecular genetic prenatal diagnosis of congenital adrenalhyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization

Phyllis W. Speiser, Perrin C. White, Jakob Dupont, Deguang Zhu, Arlene Mercado, Maria I. New

Research output: Contribution to journal › Article › peer-review

9 Scopus citations

Fingerprint

Dive into the research topics of 'Molecular genetic prenatal diagnosis of congenital adrenalhyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization'. Together they form a unique fingerprint.

Medicine & Life Sciences