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[Antenatal detection of congenital adrenal hyperplasia. Deficiency of 21-hydroxylase].

作者信息

Floret D, Plauchu H, Berlin F, Betuel H, Forest M

出版信息

Nouv Presse Med. 1980 Jun 28;9(28):1960-1.

PMID:6968432
Abstract
摘要

相似文献

1
[Antenatal detection of congenital adrenal hyperplasia. Deficiency of 21-hydroxylase].
Nouv Presse Med. 1980 Jun 28;9(28):1960-1.
2
Amniotic 17-alpha hydroxyprogesterone and HLA typing for the prenatal diagnosis of 21-alpha hydroxylase deficiency--congenital adrenal hyperplasia.羊水中17-α羟孕酮及HLA分型用于21-α羟化酶缺乏症（先天性肾上腺皮质增生症）的产前诊断
Am J Med Genet. 1980;6(4):295-300. doi: 10.1002/ajmg.1320060406.
3
[Antenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
Rev Prat. 1991 May 1;41(13):1183-7.
4
[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.
5
[Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
J Genet Hum. 1981 Mar;29(1):103-13.
6
[The eugenic significance of HLA determination in congenital adrenal hyperplasia].
Zhonghua Yi Xue Za Zhi. 1984 Feb;64(2):105-7.
7
[Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies].[21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前治疗。9例接受治疗的妊娠]
Ann Pediatr (Paris). 1993 Sep;40(7):421-5.
8
[Possibilities of prenatal diagnosis of the adrenogenital syndrome using HLA typing of cultivated amnion cells].
Dtsch Med Wochenschr. 1979 Apr 6;104(14):526.
9
Congenital adrenal hyperplasia.
J Singapore Paediatr Soc. 1991;33(3-4):117-25.
10
[Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers].
Lijec Vjesn. 1983 Apr;105(4):145-9.