INTRAGENIC DELETIONS IN 21 DUCHENNE MUSCULAR-DYSTROPHY (DMD) BECKER MUSCULAR-DYSTROPHY (BMD) FAMILIES STUDIED WITH THE DYSTROPHIN CDNA - LOCATION OF BREAKPOINTS ON HINDIII AND BGIII EXON-CONTAINING FRAGMENT MAPS, MEIOTIC AND MITOTIC ORIGIN OF THE MUTATIONS

被引：0

作者：

DARRAS, BT

BLATTNER, P

HARPER, JF

SPIRO, AJ

ALTER, S

FRANCKE, U

机构：

[1] YALE UNIV,SCH MED,DEPT HUMAN GENET,333 CEDAR ST,NEW HAVEN,CT 06510

[2] WHITE PLAINS HOSP,MDA CLIN,NEW YORK,NY

[3] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT NEUROL,BRONX,NY 10461

[4] WESTCHESTER HOSP,MDA CLIN,NEW YORK,NY

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D O I：

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中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：620 / 629

页数：10