Literature DB >> 9238271

21-hydroxylase deficiency.

R S Newfield1, M I New.   

Abstract

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Mesh：

Year:  1997        PMID： 9238271     DOI： 10.1111/j.1749-6632.1997.tb52145.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.  Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis.

Authors:  M Lako; S Ramsden; R D Campbell; T Strachan
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

2.  Circadian rise in maternal glucocorticoid prevents pulmonary dysplasia in fetal mice with adrenal insufficiency.

Authors:  M Venihaki; A Carrigan; P Dikkes; J A Majzoub
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

3.  In Vitro Enzyme Assay of CYP21A2 Mutation (R483Q) by A Novel Method Using Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS).

Authors:  Makoto Ono; Kenichi Kashimada; Kentaro Miyai; Toshikazu Onishi; Masatoshi Takagi; Seijiro Honma; Shuki Mizutani
Journal:  Clin Pediatr Endocrinol       Date:  2008-05-08
  3 in total

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