HLA and congenital adrenal hyperplasia linkage confirmed.

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Lancet. 1978 Apr 29;1(8070):930-2.

PMID:76861

Abstract

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相似文献

HLA and congenital adrenal hyperplasia linkage confirmed.

Lancet. 1978 Apr 29;1(8070):930-2.

HLA and congenital adrenal hyperplasia.人类白细胞抗原与先天性肾上腺皮质增生症

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

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

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HLA and congenital adrenal hyperplasia.人类白细胞抗原与先天性肾上腺皮质增生症

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HLA typing of amniotic-fluid cells applied to prenatal diagnosis of congenital adrenal hyperplasia.羊水细胞的HLA分型应用于先天性肾上腺皮质增生症的产前诊断。

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Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group.HLA连锁群内21-羟化酶缺陷基因的遗传定位。

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Mapping of the 21-hydroxylase deficiency gene within the HLA linkage group.21-羟化酶缺乏症基因在HLA连锁群中的定位。

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Genetics of acquired and congenital adrenal hyperplasia.获得性和先天性肾上腺增生的遗传学

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Prenatal diagnosis of congenital adrenal hyperplasia.

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引用本文的文献

Linkage and association between HLA and 21-hydroxylase deficiency.HLA与21-羟化酶缺乏症之间的连锁与关联。

J Med Genet. 1980 Oct;17(5):337-41. doi: 10.1136/jmg.17.5.337.

Genetics of ambiguous genitalia.

Indian J Pediatr. 1982 Mar-Apr;49(397):277-80. doi: 10.1007/BF02830767.

Congenital adrenal hyperplasia--a clinical and genetic survey. Are we detecting male salt-losers?先天性肾上腺皮质增生症——一项临床与遗传学调查。我们是否检测出男性失盐型患者？

Arch Dis Child. 1980 Aug;55(8):622-5. doi: 10.1136/adc.55.8.622.

Data on linkage relations between GLO and 21-hydroxylase.

Hum Genet. 1980;54(3):419-20. doi: 10.1007/BF00291592.

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

Hum Genet. 1980;53(3):389-92. doi: 10.1007/BF00287061.

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.HLA连锁以及B14、DR1、BfS单倍型与迟发性和隐匿性21-羟化酶缺乏症相关基因的关联。

Am J Hum Genet. 1981 Jul;33(4):540-50.

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.

Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.脉冲场凝胶电泳显示，在21-羟化酶缺乏单倍型中，串联的21-羟化酶和补体C4基因重复序列数量存在高度变异性。

EMBO J. 1989 May;8(5):1393-402. doi: 10.1002/j.1460-2075.1989.tb03520.x.

21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.具有HLA相同的患病和未患病同胞的21-羟化酶缺乏症家族。

J Med Genet. 1989 Jan;26(1):10-7. doi: 10.1136/jmg.26.1.10.

Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families.爱尔兰21-羟化酶缺乏症家族中的扩展MHC单倍型和CYP21/C4基因组织

Hum Genet. 1991 Jul;87(3):361-6. doi: 10.1007/BF00200920.

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