FAMILIAL DELETION OF XP21.2 WITH GLYCEROL KINASE-DEFICIENCY AND CONGENITAL ADRENAL HYPOPLASIA

被引：13

作者：

MARLHENS, F

CHELLY, J

KAPLAN, JC

LEFRANCOIS, D

HARPEY, JP

DUTRILLAUX, B

机构：

[1] INST CURIE, BIOL SECT, CNRS, UA 620, 26 RUE ULM, F-75231 PARIS 05, FRANCE

[2] CHU COCHIN, INST PATHOL MOLEC, INSERM, U129, F-75014 PARIS, FRANCE

[3] GRP HOSP PITIE SALPETRIERE, PEDIAT GENET MED CLIN, F-75651 PARIS 13, FRANCE

来源：

HUMAN GENETICS | 1987年 / 77卷 / 04期

关键词：

D O I：

10.1007/BF00291430

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：379 / 383

页数：5

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