Literature DB >> 6980498

HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population.

P Couillin, R Rappaport, F Kuttenn, P Canlorbe, J Hors, A Marcelli-Barge, J Feingold, M C Grisard, J Boué, A Boué.   

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Year:  1982        PMID： 6980498     DOI： 10.1111/j.1399-0039.1982.tb01424.x

Source DB:  PubMed          Journal:  Tissue Antigens        ISSN： 0001-2815


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  4 in total

1.  The immunological detection of a 21-OH deficiency mutation HLA supratype.

Authors:  M S Pollack; B Keenan; F T Christiansen; T J Cobain; R L Dawkins; G Clayton
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

2.  First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.

Authors:  E Mornet; J Boue; M Raux-Demay; P Couillin; J F Oury; Y Dumez; J Dausset; D Cohen; A Boué
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

3.  Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.

Authors:  J Partanen; S Koskimies; I Sipilä; V Lipsanen
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

4.  Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency.

Authors:  E Mornet; P Couillin; F Kutten; M C Raux; P C White; D Cohen; A Boué; J Dausset
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132
  4 in total

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