HIGH-RESOLUTION CHROMOSOME ANALYSIS AND FLUORESCENCE IN-SITU HYBRIDIZATION IN PATIENTS REFERRED FOR PRADER-WILLI OR ANGELMAN SYNDROME

被引：12

作者：

BUTLER, MG ^{[1
]}

机构：

[1] VANDERBILT UNIV,SCH MED,DEPT PEDIAT & PATHOL,NASHVILLE,TN 37212

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 56卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320560414

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：420 / 422

页数：3

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