FAMILIAL PRADER-WILLI SYNDROME WITH APPARENTLY NORMAL CHROMOSOMES

被引：27

作者：

LUBINSKY, M

ZELLWEGER, H

GREENSWAG, L

LARSON, G

HANSMANN, I

LEDBETTER, D

机构：

[1] UNIV IOWA HOSP & CLIN,DEPT PEDIAT,IOWA CITY,IA 52242

[2] UNIV NEBRASKA,MED CTR,OMAHA,NE 68105

[3] CHILDRENS MEM HOSP,OMAHA,NE

[4] GLENWOOD STATE HOSP SCH,GLENWOOD,IA

[5] BAYLOR COLL MED,HOUSTON,TX 77030

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 01期

关键词：

D O I：

10.1002/ajmg.1320280106

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：37 / 43

页数：7

共 27 条

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[6]

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[8]

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

[9] DEFICIENCY, TRANSPOSITION, AND DUPLICATION OF ONE 15Q REGION MAY BE ALTERNATIVELY ASSOCIATED WITH PRADER-WILLI (OR A SIMILAR) SYNDROME - ANALYSIS OF 7 CASES AFTER VARYING ASCERTAINMENT [J].

FRACCARO, M ;

ZUFFARDI, O ;

BUHLER, E ;

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SIMONI, G ;

WITKOWSKI, R ;

BONIFACI, E ;

CAUFIN, D ;

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[10]

Gorlin R J, 1979, Birth Defects Orig Artic Ser, V15, P181

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