DELETION PROXIMAL TO DXS68 LOCUS (L1-PROBE SITE) IN A BOY WITH DUCHENNE MUSCULAR-DYSTROPHY, GLYCEROL KINASE-DEFICIENCY, AND ADRENAL HYPOPLASIA

被引：25

作者：

CHELLY, J

MARLHENS, F

DUTRILLAUX, B

VANOMMEN, GJ

LAMBERT, M

HAIOUN, B

BOISSINOT, G

FARDEAU, M

KAPLAN, JC

机构：

[1] CHU COCHIN,INST PATHOL MOLEC,INSERM,U129,24 RUE FAUBOURG ST JACQUES,F-75014 PARIS,FRANCE

[2] STATE UNIV LEIDEN,SYLVIUS LABS,DEPT HUMAN GENET,2330 AL LEIDEN,NETHERLANDS

[3] CHR MEAUX,BIOCHIM LAB,F-77000 MEAUX,FRANCE

[4] HOP CITE UNIV,F-75014 PARIS,FRANCE

[5] INST CURIE,CNRS,UNITE 6720,F-75231 PARIS 05,FRANCE

[6] INSERM,U153,F-75005 PARIS,FRANCE

来源：

HUMAN GENETICS | 1988年 / 78卷 / 03期

关键词：

D O I：

10.1007/BF00291665

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：222 / 227

页数：6

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