HLA and congenital adrenal hyperplasia due to 11-hydroxylase deficiency.
作者信息
Glenthøj A, Nielsen M D, Starup J, Svejgaard A
出版信息
Tissue Antigens. 1979 Aug;14(2):181-2. doi: 10.1111/j.1399-0039.1979.tb00839.x.
Abstract
摘要
相似文献
1
HLA and congenital adrenal hyperplasia due to 11-hydroxylase deficiency.HLA与11β-羟化酶缺乏所致先天性肾上腺皮质增生症
Tissue Antigens. 1979 Aug;14(2):181-2. doi: 10.1111/j.1399-0039.1979.tb00839.x.
2
Detection of heterozygote of 21-hydroxylase deficiency.
Lancet. 1980 Jan 5;1(8158):47. doi: 10.1016/s0140-6736(80)90585-1.
3
[Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].
Lijec Vjesn. 1983 Jul-Aug;105(7-8):290-2.
4
Genetic linkage and HLA association in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Hum Immunol. 1983 May;7(1):35-44. doi: 10.1016/0198-8859(83)90005-8.
5
[HL-A associated inheritance of the 21-hydroxylase defect in familial adrenogenital syndrome].[家族性肾上腺性征异常综合征中21-羟化酶缺陷与HL-A的关联遗传]
Verh Dtsch Ges Inn Med. 1978(84):1412-6.
6
Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).
Lancet. 1977;2(8052-8053):1309-12. doi: 10.1016/s0140-6736(77)90362-2.
7
[Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)].
Pediatr Med Chir. 1981 Jul-Aug;3(4):287-90.
8
Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency confirmed by HLA tissue typing.
Acta Endocrinol (Copenh). 1979 Nov;92(3):542-6. doi: 10.1530/acta.0.0920542.
9
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.
10
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.
引用本文的文献
1
The human genome through the eyes of Mercator and Vesalius.从墨卡托和维萨里的视角看人类基因组。
Trans Am Clin Climatol Assoc. 1981;92:66-90.
2
Congenital adrenal hyperplasia due to combined 21- and 11 beta-hydroxylase deficiency.由21-羟化酶和11β-羟化酶联合缺乏所致的先天性肾上腺增生症。
J Endocrinol Invest. 1989 Nov;12(10):723-8. doi: 10.1007/BF03350043.
Zotero 插件