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

页码：159 / 177

页数：19

共 27 条

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[2]

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[3]

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KUROKI, Y ;

MATSUI, I ;

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[5]

FALEK A, 1966, PEDIATRICS, V37, P92

[6] FAMILIAL PARTIAL TRISOMY OF THE LONG ARM OF CHROMOSOME-3 (3Q) [J].

FEAR, C ;

BRIGGS, A .

ARCHIVES OF DISEASE IN CHILDHOOD, 1979, 54 (02) :135-138

[7]

FINEMAN RM, 1978, PEDIATRICS, V61, P611

[8]

Francke U, 1978, Birth Defects Orig Artic Ser, V14, P191

[9] CHROMOSOME 3Q DUPLICATION AND THE BRACHMANN-DELANGE SYNDROME (BDLS) [J].

FRANCKE, U ;

OPITZ, JM .

JOURNAL OF PEDIATRICS, 1979, 95 (01) :161-162

[10] PARTIAL TRISOMY FOR LONG ARM OF CHROMOSOME-3 [3(Q21-]QTER)+] IN A NEWBORN WITH MINOR PHYSICAL STIGMATA [J].

FRYNS, JP ;

VANEYGEN, M ;

LOGGHE, N ;

VANDENBERGHE, H .

HUMAN GENETICS, 1978, 40 (03) :333-339

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