LOCALIZATION AND CLONING OF XP21 DELETION BREAKPOINTS INVOLVED IN MUSCULAR-DYSTROPHY

被引：133

作者：

MONACO, AP

BERTELSON, CJ

COLLETTIFEENER, C

KUNKEL, LM

机构：

[1] CHILDRENS HOSP MED CTR,DIV GENET,300 LONGWOOD AVE,BOSTON,MA 02115

[2] HARVARD UNIV,PROGRAM NEUROSCI,CAMBRIDGE,MA 02138

来源：

关键词：

D O I：

10.1007/BF00281063

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：221 / 227

页数：7

共 33 条

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