Literature DB >> 6966250

HLA-A, B, C, DR alleles in congenital adrenal hyperplasia.

P Couillin, M L Kottler-Missonnier, M C Grisard, J Hors, J Feingold, J Boué, A Boué.   

Abstract

HLA markers (A, B, C, DR loci) were determined for the members of 52 unrelated families with at least one child suffering from congenital adrenal hyperplasia due to 21 hydroxylase deficiency, permitting genotyping. The gene frequencies of the 52 index cases were compared with those obtained from the patients' normal haplotypes and with those of a control reference panel. No significant differences were observed, except a clear decrease in the frequency of HLA-B8 among the haplotypes that carry the gene for congenital adrenal hyperplasia.

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Year:  1980        PMID： 6966250     DOI： 10.1007/BF00287061

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  8 in total

1.  Serotyping for homotransplantation. 18. Refinement of microdroplet lymphocyte cytotoxicity test.

Authors:  K K Mittal; M R Mickey; D P Singal; P I Terasaki
Journal:  Transplantation       Date:  1968-11       Impact factor: 4.939

2.  A haplotype study of HLA complex with special reference to the HLA-DR series and to Bf. C2 and glyoxalase I polymorphisms.

Authors:  J Dausset; L Legrand; V Lepage; L Contu; A Marcelli-Barge; I Wildloecher; A Benajam; T Meo; L Degos
Journal:  Tissue Antigens       Date:  1978-10

3.  HLA typing of amniotic-fluid cells applied to prenatal diagnosis of congenital adrenal hyperplasia.

Authors:  P Couillin; H Nicolas; J Boué; A Boué
Journal:  Lancet       Date:  1979-05-19       Impact factor: 79.321

4.  HLA and congenital adrenal hyperplasia linkage confirmed.

Authors: 
Journal:  Lancet       Date:  1978-04-29       Impact factor: 79.321

5.  Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group.

Authors:  L S Levine; M Zachmann; M I New; A Prader; M S Pollack; G J O'Neill; S Y Yang; S E Oberfield; B Dupont
Journal:  N Engl J Med       Date:  1978-10-26       Impact factor: 91.245

6.  HLA in populations: an approach for genetical susceptibility to cancer.

Authors:  N Feingold; L Degos; J Feingold
Journal:  J Immunogenet       Date:  1979-02

7.  Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.

Authors:  M S Pollack; D Maurer; L S Levine; M I New; S Pang; M Duchon; R P Owens; I R Merkatz; B M Nitowsky; G Sachs; B Dupont
Journal:  Lancet       Date:  1979-05-26       Impact factor: 79.321

8.  Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

Authors:  B Dupont; S E Oberfield; E M Smithwick; T D Lee; L S Levine
Journal:  Lancet       Date:  1977 Dec 24-31       Impact factor: 79.321
  8 in total
  1 in total

1.  HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency.

Authors:  M S Pollack; M I New; G J O'Neill; L S Levine; C Callaway; S Pang; E Cacciari; F Mantero; A Cassio; C Scaroni; G Chiumello; G F Rondanini; L Gargantini; G Giovannelli; R Virdis; E Bartolotta; C Migliori; C Pintor; L Tato; F Barboni; B Dupont
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  1 in total

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