Literature DB >> 6244326

Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

F Lorenzen, S Pang, M New, M Pollack, S Oberfield, B Dupont, D Chow, B Schneider, L Levine.   

Abstract

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Year:  1980        PMID： 6244326     DOI： 10.1210/jcem-50-3-572

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


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  5 in total

1.  17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies.

Authors:  C Scaroni; A Biason; G Carpenè; G Opocher; F Mantero
Journal:  J Endocrinol Invest       Date:  1991-02       Impact factor: 4.256

2.  High frequency of nonclassical steroid 21-hydroxylase deficiency.

Authors:  P W Speiser; B Dupont; P Rubinstein; A Piazza; A Kastelan; M I New
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

3.  Intersex problems in the neonate.

Authors:  R K Danish
Journal:  Indian J Pediatr       Date:  1982 Jul-Aug       Impact factor: 1.967

4.  Detection of late onset steroid 21-hydroxylase deficiency by capillary gas chromatographic profiling of urinary steroids in children and adolescents.

Authors:  J Homoki; J Solyom; W M Teller
Journal:  Eur J Pediatr       Date:  1988-04       Impact factor: 3.183

5.  HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.

Authors:  P C White; M I New; B Dupont
Journal:  Proc Natl Acad Sci U S A       Date:  1984-12       Impact factor: 11.205
  5 in total

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