DUPLICATION 8Q SYNDROME DUE TO FAMILIAL CHROMOSOME INS(10-8)(Q21-Q212Q22)

被引：11

作者：

BOWEN, P

FITZGERALD, PH

GARDNER, RJM

BIEDERMAN, B

VEALE, AMO

机构：

[1] CHRISTCHURCH HOSP,CYTOGENET UNIT,CHRISTCHURCH,NEW ZEALAND

[2] DUNEDIN HOSP,DEPT PEDIAT & CHILD HLTH,DUNEDIN,NEW ZEALAND

[3] UNIV OTAGO,SCH MED,DUNEDIN,NEW ZEALAND

[4] UNIV AUCKLAND,DEPT COMMUNITY HLTH,AUCKLAND,NEW ZEALAND

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1983年 / 14卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320140407

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：635 / 646

页数：12

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[3]

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[4]

FINEMAN RM, 1979, CLIN GENET, V16, P390

[5]

ISCN An international system for human cytogenetic nomen-clature, 1978, CYTOGENET CELL GENET, V21, P309

[6]

PFEIFFER RA, 1977, NEW CHROMOSOMAL SYND

[7]

Riccardi V M, 1977, Birth Defects Orig Artic Ser, V13, P171

[8] KARYOTYPE-PHENOTYPE CORRELATION - MOSAIC TRISOMY-8 AND PARTIAL TRISOMIES OF DIFFERENT SEGMENTS OF CHROMOSOME-8 [J].

RICCARDI, VM ;

CRANDALL, BF .

HUMAN GENETICS, 1978, 41 (03) :363-365

[9] PARTIAL TRISOMY 8 (8Q24) AND TRISOMY-8 SYNDROME [J].

SANCHEZ, O ;

YUNIS, JJ .

HUMANGENETIK, 1974, 23 (04) :297-303

[10] PARTIAL TRISOMY-8Q IN HALF-SISTERS WITH DISTINCT DYSMORPHIC PATTERNS NOT SIMILAR TO TRISOMY-8 MOSAICISM SYNDROME [J].

SCHINZEL, A .

HUMAN GENETICS, 1977, 37 (01) :17-26

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