Literature DB >> 7218273

Linkage and association between HLA and 21-hydroxylase deficiency.

P T Klouda, R Harris, D A Price.   

Abstract

Congenital adrenal hyperplasia because of 21-hydroxylase deficiency is closely linked to the HLA system. The lod scores in 14 informative families are presented. Apart from linkage, the 21-hydroxylase deficiency is associated with an increase of BW47 antigen and lack of B8 antigen in patients. A family with a possible recombination between the 21-hydroxylase deficiency and the HLA complex was found, thus indicating that the 21-hydroxylase gene lies outside the HLA system and is closely linked to the HLA-DR locus.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7218273      PMCID: PMC1048595          DOI: 10.1136/jmg.17.5.337

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  The estimation of pregnanetriol and 17-hydroxypregnanolone in urine in congenital adrenal hyperplasia.

Authors:  M BELL; H VARLEY
Journal:  Clin Chim Acta       Date:  1960-05       Impact factor: 3.786

2.  Maternal age and Down's syndrome.

Authors: 
Journal:  Lancet       Date:  1978-07-01       Impact factor: 79.321

3.  HLA and congenital adrenal hyperplasia linkage confirmed.

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

4.  Transient hypoxaemia during sleep in chronic bronchitis and emphysema.

Authors:  N J Douglas; P M Calverley; R J Leggett; H M Brash; D C Flenley; V Brezinova
Journal:  Lancet       Date:  1979-01-06       Impact factor: 79.321

5.  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

  5 in total
  5 in total

Review 1.  The Gordon Wilson Lecture. Congenital adrenal hyperplasia.

Authors:  M I New
Journal:  Trans Am Clin Climatol Assoc       Date:  1991

2.  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

3.  Genetics and biochemical variability of variants of 21 hydroxylase deficiency.

Authors:  M T Gordon; D I Conway; D C Anderson; R Harris
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

4.  HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

Authors:  M S Pollack; L S Levine; G J O'Neill; S Pang; F Lorenzen; B Kohn; G F Rondanini; G Chiumello; M I New; B Dupont
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025

5.  The biochemical basis for genotyping 21-hydroxylase deficiency.

Authors:  M I New; B Dupont; M S Pollack; L S Levine
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.