Literature DB >> 3879117

Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.

S Pang, M S Pollack, M Loo, O Green, R Nussbaum, G Clayton, B Dupont, M I New.   

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Year:  1985        PMID： 3879117     DOI： 10.1111/j.1749-6632.1985.tb14597.x

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


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  3 in total

1.  Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.

Authors:  E Passarge
Journal:  Indian J Pediatr       Date:  1988 Jul-Aug       Impact factor: 1.967

2.  First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.

Authors:  E Mornet; J Boue; M Raux-Demay; P Couillin; J F Oury; Y Dumez; J Dausset; D Cohen; A Boué
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

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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