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HLA typing of amniotic-fluid cells applied to prenatal diagnosis of congenital adrenal hyperplasia.

作者信息

Couillin P, Nicolas H, Boué J, Boué A

出版信息

Lancet. 1979 May 19;1(8125):1076. doi: 10.1016/s0140-6736(79)92966-0.

DOI:10.1016/s0140-6736(79)92966-0
PMID:86789
Abstract
摘要

相似文献

1
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。
Lancet. 1979 May 19;1(8125):1076. doi: 10.1016/s0140-6736(79)92966-0.
2
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.
Lancet. 1979 May 26;1(8126):1107-8. doi: 10.1016/s0140-6736(79)91789-6.
3
[Methodology for HLA typing of amniotic fluid fetal cells (author's transl)].
Ann Genet. 1980;23(1):40-5.
4
The use of gamma interferon to increase HLA antigen expression on cultured amniotic cells used for the prenatal diagnosis of 21-hydroxylase deficiency.使用γ干扰素增加用于21-羟化酶缺乏症产前诊断的培养羊膜细胞上的HLA抗原表达。
Ann N Y Acad Sci. 1985;458:148-55. doi: 10.1111/j.1749-6632.1985.tb14599.x.
5
HLA and congenital adrenal hyperplasia linkage confirmed.
Lancet. 1978 Apr 29;1(8070):930-2.
6
Technical and theoretical considerations in the HLA typing of amniotic fluid cells for prenatal diagnosis and paternity testing.用于产前诊断和亲子鉴定的羊水细胞HLA分型中的技术和理论考量
Prenat Diagn. 1981 Jul;1(3):183-95. doi: 10.1002/pd.1970010304.
7
[Prenatal detection of congenital adrenal hyperplasia using HLA typing of fetal cells from the amniotic fluid].
Lijec Vjesn. 1986 Nov-Dec;108(11-12):497-500.
8
HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency.用于补体C4缺乏症产前诊断的培养羊膜细胞的HLA分型
Clin Genet. 1980 Sep;18(3):197-200. doi: 10.1111/j.1399-0004.1980.tb00871.x.
9
HLA typing by serology and by molecular biology of fetal and cord-blood cells.
Bone Marrow Transplant. 1992;9 Suppl 1:60-3.
10
Prenatal diagnosis of congenital adrenal hyperplasia (21-OH deficiency type) by HLA typing.通过HLA分型对先天性肾上腺皮质增生症（21-羟化酶缺乏型）进行产前诊断。
Prenat Diagn. 1981 Jan;1(1):25-33. doi: 10.1002/pd.1970010107.

引用本文的文献

1
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot.通过等位基因特异性杂交和Southern印迹法对21-羟化酶缺乏所致先天性肾上腺皮质增生症进行产前诊断。
Hum Genet. 1994 Apr;93(4):424-8. doi: 10.1007/BF00201668.
2
Congenital adrenal hyperplasia associated with a balanced 13--18 translocation.与13号和18号染色体平衡易位相关的先天性肾上腺皮质增生症。
Eur J Pediatr. 1980 May;133(3):283-5. doi: 10.1007/BF00496091.
3
Location of the gene for 21-hydroxylase deficiency.21-羟化酶缺乏症基因的定位
J Med Genet. 1980 Dec;17(6):447-52. doi: 10.1136/jmg.17.6.447.
4
HLA-A, B, C, DR alleles in congenital adrenal hyperplasia.
Hum Genet. 1980;53(3):389-92. doi: 10.1007/BF00287061.
5
Comments on some genetic abnormalities of sex determination and sex differentiation in Homo sapiens.关于人类性别决定和性别分化的一些遗传异常的评论
Eur J Pediatr. 1980 Mar;133(2):77-91. doi: 10.1007/BF00441575.
6
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.
7
The Gordon Wilson Lecture. Congenital adrenal hyperplasia.戈登·威尔逊讲座。先天性肾上腺皮质增生症
Trans Am Clin Climatol Assoc. 1991;102:108-22.