Phenotypic evolution of classic 21-hydroxylase deficiency-Reference-Cited by-同舟云学术

Phenotypic evolution of classic 21-hydroxylase deficiency

Published:1996-07 Issue:1 Volume:45 Page:103-109
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Hoffman William H.,Shln Myung Y.,Donohoue Patricia A.,Helman Sandra W.,Brown Stephanle L.,Rosculet George,Mahesh Virendra B.

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.1996.tb02067.x/fullpdf

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4. Difference in transcriptional activity of two homologous CYP21A genes;Chang;Molecular Endocrinolog,1995

5. Aldosterone and cortisol secretion rates in infants and children with congenital adrenal hyperplasia suggesting different 21-hydroxylation defects in salt-losers and nonsalt-lowers;Degenhart;Acta Endocrinologica,1965

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