DUCHENNE MUSCULAR-DYSTROPHY DUE TO FAMILIAL XP21 DELETION DETECTABLE BY DNA ANALYSIS AND FLOW-CYTOMETRY

被引：41

作者：

WILCOX, DE ^{[1
]}

COOKE, A ^{[1
]}

COLGAN, J ^{[1
]}

BOYD, E ^{[1
]}

AITKEN, DA ^{[1
]}

SINCLAIR, L ^{[1
]}

GLASGOW, L ^{[1
]}

STEPHENSON, JB ^{[1
]}

FERGUSONSMITH, MA ^{[1
]}

机构：

[1] ROYAL HOSP SICK CHILDREN,FRASER ALLANDER ASSESSMENT UNIT,GLASGOW G3 8SJ,SCOTLAND

来源：

HUMAN GENETICS | 1986年 / 73卷 / 02期

关键词：

D O I：

10.1007/BF00291610

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：175 / 180

页数：6

共 19 条

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