HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France. - Suppr | 超能文献

HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France.

作者信息

Couillin P, Rappaport R, Kuttenn F, Hors J, Feingold J, Boué J, Boué A

出版信息

Ann N Y Acad Sci. 1985;458:41-5. doi: 10.1111/j.1749-6632.1985.tb14588.x.

DOI:10.1111/j.1749-6632.1985.tb14588.x

Abstract

摘要

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HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France.

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HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population.法国人群中的人类白细胞抗原（HLA）与21-羟化酶缺乏症（先天性及迟发性肾上腺皮质增生症）

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The HLA associations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a Yugoslav population.

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The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes.以特定主要组织相容性复合体超型为特征的IgA缺乏症与21-羟化酶缺乏症共存。

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HLA-B14 and nonclassical 21-hydroxylase deficiency in a heterogeneous New York population.纽约异质人群中的HLA - B14与非经典21 - 羟化酶缺乏症

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引用本文的文献

1

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.通过与HLA - DNA探针的连锁分析及17 - 羟孕酮测定对孕早期21 - 羟化酶缺乏症进行产前诊断。

Hum Genet. 1986 Aug;73(4):358-64. doi: 10.1007/BF00279101.