CONFERENCE REPORT - 2ND ANNUAL PRADER-WILLI SYNDROME SCIENTIFIC CONFERENCE

被引：26

作者：

LEDBETTER, DH

GREENBERG, F

HOLM, VA

CASSIDY, SB

机构：

[1] BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030

[2] UNIV WASHINGTON,SCH MED,CTR CHILD DEV & MENTAL RETARDAT,DEPT PEDIAT,SEATTLE,WA 98195

[3] UNIV CONNECTICUT,SCH MED,DEPT PEDIAT,DIV HUMAN GENET,FARMINGTON,CT 06032

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320280402

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：779 / 790

页数：12

共 21 条

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[3] DELETION OF CHROMOSOME-15 (Q11-13) IN A PRADER-LABHART-WILLI SYNDROME CLINIC POPULATION [J].

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[5]

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[7] ISOLATION OF MOLECULAR PROBES ASSOCIATED WITH THE CHROMOSOME-15 INSTABILITY IN THE PRADER-WILLI SYNDROME [J].

DONLON, TA ;

LALANDE, M ;

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BRUNS, G ;

LATT, SA .

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[8]

FEAR CN, 1985, DEV MED CHILD NEUROL, V27, P305

[9]

Fukui S., 1984, ADV BIOCHEM ENG BIOT, V29, P1, DOI DOI 10.1007/BFB0000689

[10] CYTOGENETIC STUDIES OF FAMILIAL PRADER-WILLI SYNDROME [J].

HASEGAWA, T ;

HARA, M ;

ANDO, M ;

OSAWA, M ;

FUKUYAMA, Y ;

TAKAHASHI, M ;

YAMADA, K .

HUMAN GENETICS, 1984, 65 (04) :325-330

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