Literature DB >> 3911845

Clinical and endocrinological aspects of 21-hydroxylase deficiency.

M I New.   

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Year:  1985        PMID: 3911845     DOI: 10.1111/j.1749-6632.1985.tb14585.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


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  3 in total

Review 1.  Diagnosis and management of ambiguous genitalia.

Authors:  L D Sherman
Journal:  Indian J Pediatr       Date:  1997 Mar-Apr       Impact factor: 1.967

2.  Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.

Authors:  P M Schneider; M C Carroll; C A Alper; C Rittner; A S Whitehead; E J Yunis; H R Colten
Journal:  J Clin Invest       Date:  1986-09       Impact factor: 14.808

3.  Prenatal diagnosis of congenital adrenal hyperplasia: reliability of amniotic fluid steroid analysis.

Authors:  I A Hughes; J Dyas; D Riad-Fahmy; K M Laurence
Journal:  J Med Genet       Date:  1987-06       Impact factor: 6.318

  3 in total

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