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
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
收藏
页码:222 / 227
页数:6
相关论文
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