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） - Suppr

Suppr

超能文献

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

作者信息

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

出版信息

Tissue Antigens. 1982 Feb;19(2):100-7. doi: 10.1111/j.1399-0039.1982.tb01424.x.

DOI:10.1111/j.1399-0039.1982.tb01424.x

PMID:6980498

Abstract

摘要

相似文献

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）

Tissue Antigens. 1982 Feb;19(2):100-7. doi: 10.1111/j.1399-0039.1982.tb01424.x.

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

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

No linkage between HLA and congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency.

N Engl J Med. 1980 Aug 28;303(9):530. doi: 10.1056/nejm198008283030923.

[Genetic of the 21 hydroxylase deficiency].[21-羟化酶缺乏症的遗传学]

Ann Endocrinol (Paris). 1982;43(1):3-14.

[Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].

J Genet Hum. 1981 Mar;29(1):103-13.

No linkage between HLA and congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency.

N Engl J Med. 1983 Apr 21;308(16):970-1. doi: 10.1056/NEJM198304213081621.

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

Ann N Y Acad Sci. 1985;458:65-70. doi: 10.1111/j.1749-6632.1985.tb14591.x.

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

Ann N Y Acad Sci. 1985;458:36-40. doi: 10.1111/j.1749-6632.1985.tb14587.x.

The association between congenital adrenal hyperplasia and HLA in Southern Italy.

Ann N Y Acad Sci. 1985;458:46-51. doi: 10.1111/j.1749-6632.1985.tb14589.x.

[HLA and congenital genital adrenal syndrome caused by 21-hydroxylase deficiency].

Minerva Pediatr. 1985 Sep 30;37(18):696-7.

引用本文的文献

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.

The immunological detection of a 21-OH deficiency mutation HLA supratype.21-羟化酶缺乏突变 HLA 超型的免疫学检测

Am J Hum Genet. 1986 May;38(5):688-98.

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency.用人类21-羟化酶（21-OH）探针检测到的限制性片段长度多态性与21-OH缺乏症的两种临床形式之间的关联。

Hum Genet. 1986 Dec;74(4):402-8. doi: 10.1007/BF00280494.

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.单一人群中经典型先天性肾上腺皮质增生症患者的主要组织相容性复合体基因标记以及类固醇21-羟化酶（CYP21）和补体C4基因的限制性片段分析

Am J Hum Genet. 1989 May;44(5):660-70.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验