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Molecular Genetics of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency): Implications for Diagnosis, Prognosis and Treatment

โœ Scribed by Wedell, A.


Book ID
122741201
Publisher
Lippincott Williams and Wilkins
Year
1998
Tongue
English
Weight
121 KB
Volume
160
Category
Article
ISSN
0022-5347

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๐Ÿ“œ SIMILAR VOLUMES


Prenatal diagnosis of congenital adrenal
โœ Dumic, M.; Brkljacic, L.; Plavsic, V.; Zunec, R.; Ille, J.; Wilson, R. C.; Kuvac ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 71 KB ๐Ÿ‘ 2 views

We report on the prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase in 20 at-risk pregnancies (16 salt-wasting and 4 simple virilizing families). We have diagnosed 3 affected fetuses (2 males and 1 female), 3 healthy homozygotes (2 males and 1 female), and 14 healthy heterozy