Výsledky vyhledávání - "I Davidschwartz"

The importance of heteroduplexes in interpreting the results of PCR-RED diagnostic assays: Application to the analysis of mutations in the steroid 21-hydroxylase gene in a case of congenital adrenal hyperplasia

Autor: Paul G. Rothberg, I Davidschwartz, John F. Bradley, Darren W. Baker

Publikováno v: Molecular Diagnosis. 3:119-124

Background: Congenital adrenal hyperplasia (CAH) due to deficiency of steroid 21-hydroxylase (CYP21) is an autosomal recessive disease that is a major cause of ambiguous genitalia at birth in females. The milder late-onset form of the disease can cau

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::00a1997145adef4e3253c52a5399b5d8
https://doi.org/10.1016/s1084-8592(98)80060-x

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