Literature DB >> 3295546

Congenital adrenal hyperplasia (2).

P C White, M I New, B Dupont.   

Abstract

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Year:  1987        PMID： 3295546     DOI： 10.1056/NEJM198706183162506

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  24 in total

Review 1.  Novel basic and clinical aspects of congenital adrenal hyperplasia.

Authors:  D P Merke; C A Camacho
Journal:  Rev Endocr Metab Disord       Date:  2001-08       Impact factor: 6.514

Review 2.  Hirsutism: pilosebaceous unit dysregulation. Role of peripheral and glandular factors.

Authors:  V Toscano
Journal:  J Endocrinol Invest       Date:  1991-02       Impact factor: 4.256

3.  Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency.

Authors:  T Matsumoto; T Kondoh; T Kamei; M Yoshimoto; Y Tsuji; K Suzumori; R Izumi; N Iwatani; N Niikawa
Journal:  Eur J Pediatr       Date:  1988-12       Impact factor: 3.183

Review 4.  Human chromosome 8.

Authors:  S Wood
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

5.  Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

Authors:  P Sinnott; S Collier; C Costigan; P A Dyer; R Harris; T Strachan
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

6.  21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

Authors:  P J Sinnott; P A Dyer; D A Price; R Harris; T Strachan
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

Review 7.  Gene conversions, deletions, and polymorphisms in congenital adrenal hyperplasia.

Authors:  W L Miller
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

8.  Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

Authors:  P C White; A Vitek; B Dupont; M I New
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

9.  Nonsense mutation causing steroid 21-hydroxylase deficiency.

Authors:  H Globerman; M Amor; K L Parker; M I New; P C White
Journal:  J Clin Invest       Date:  1988-07       Impact factor: 14.808

10.  Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism.

Authors:  T Tajima; K Fujieda; K Nakayama; Y Fujii-Kuriyama
Journal:  J Clin Invest       Date:  1993-11       Impact factor: 14.808
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