GERMINAL MOSAICISM INCREASES THE RECURRENCE RISK FOR NEW DUCHENNE MUSCULAR-DYSTROPHY MUTATIONS

被引：163

作者：

BAKKER, E ^{[1
]}

VEENEMA, H ^{[1
]}

DENDUNNEN, JT ^{[1
]}

VAN BROECKHOVEN, C ^{[1
]}

GROOTSCHOLTEN, PM ^{[1
]}

BONTEN, EJ ^{[1
]}

VANOMMEN, GJB ^{[1
]}

PEARSON, PL ^{[1
]}

机构：

[1] UNIV INSTELLING ANTWERP, DEPT BIOCHEM, B-2610 WILRIJK, BELGIUM

来源：

JOURNAL OF MEDICAL GENETICS | 1989年 / 26卷 / 09期

关键词：

D O I：

10.1136/jmg.26.9.553

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：553 / 559

页数：7

共 28 条

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[2]

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[4]

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[8] DIRECT METHOD FOR PRENATAL-DIAGNOSIS AND CARRIER DETECTION IN DUCHENNE BECKER MUSCULAR-DYSTROPHY USING THE ENTIRE DYSTROPHIN CDNA [J].

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[9] A PARTIAL DELETION OF THE MUSCULAR-DYSTROPHY GENE TRANSMITTED TWICE BY AN UNAFFECTED MALE [J].

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[10] DIRECT DETECTION OF MORE THAN 50-PERCENT OF THE DUCHENNE MUSCULAR-DYSTROPHY MUTATIONS BY FIELD INVERSION GELS [J].

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