Direct Analysis of CYP21B Genes in 21-Hydroxylase Deficiency using Polymerase Chain Reaction Amplification
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1990
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Abstract
Abstract. Steroid 21-hydroxylase deficiency is the leading cause of impaired cortisol synthesis in congenital adrenal hyperplasia (CAH). We have studied the str
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| Authors | Owerbach, David;Crawford, Yvette M.;Draznin, Martin B.; |
| Journal | Molecular Endocrinology |
| Year | 1990 |
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