THE DUP(3Q) SYNDROME - REPORT OF 8 CASES AND REVIEW OF THE LITERATURE

被引：73
|
作者：
STEINBACH, P
ADKINS, WN
CASPAR, H
DUMARS, KW
GEBAUER, J
GILBERT, EF
GRIMM, T
HABEDANK, M
HANSMANN, I
HERRMANN, J
KAVEGGIA, EG
LANGENBECK, U
MEISNER, LF
NAJAFZADEH, TM
OPITZ, JM
PALMER, CG
PETERS, HH
SCHOLZ, W
TAVARES, AS
WIEDEKING, C
机构：
[1] RUHR UNIV BOCHUM,ARBEITSGRP HUMANCYCTOGENET & KLIN GENET,D-4630 BOCHUM,FED REP GER
[2] CENT WISCONSIN CTR DEV DISABLED,MADISON,WI
[3] ELISABETH HOSP,KINDERKLIN,RHEYDT,FED REP GER
[4] UNIV CALIF IRVINE,ORANGE CTY MED CTR,DEPT PEDIAT,DIV CLIN GENET & DEV DISABILITIES,ORANGE,CA 92668
[5] UNIV GOTTINGEN,DEPT HUMAN GENET,D-3400 GOTTINGEN,FED REP GER
[6] UNIV WISCONSIN,DEPT PATHOL,MADISON,WI 53706
[7] RHEIN WESTFAL TH AACHEN,FAK MED,D-5100 AACHEN,FED REP GER
[8] MILWAUKEE CHILDRENS HOSP,MILWAUKEE,WI 53233
[9] UNIV WISCONSIN,STATE LAB HYG,MADISON,WI 53706
[10] INDIANA UNIV,SCH MED,DEPT MED GENET,BLOOMINGTON,IN 47401
[11] UNIV GOTTINGEN,KINDERKLIN,D-3400 GOTTINGEN,FED REP GER
[12] SHODAIR CHILDRENS HOSP,HELENA,MT
[13] UNIV PORTO,FAC MED,SERV PATOL GERAL,PORTO,PORTUGAL
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1981年 / 10卷 / 02期
关键词：
D O I：
10.1002/ajmg.1320100210
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：159 / 177
页数：19
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