A TERMINAL DELETION OF THE LONG ARM OF CHROMOSOME-4 [46,XX,DEL(4)(Q33)] IN AN INFANT WITH PHENOTYPIC FEATURES OF WILLIAMS SYNDROME

被引：39

作者：

JEFFERSON, RD

BURN, J

GAUNT, KL

HUNTER, S

DAVISON, EV

机构：

[1] UNIV NEWCASTLE UPON TYNE,DEPT HUMAN GENET,19 CLAREMONT PL,NEWCASTLE TYNE NE2 4AA,ENGLAND

[2] FREEMAN HOSP,REG PAEDIAT CARDIOL UNIT,NEWCASTLE TYNE NE7 7DN,TYNE & WEAR,ENGLAND

来源：

关键词：

D O I：

10.1136/jmg.23.5.474

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：474 / 477

页数：4

共 24 条

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BINGHAM, W
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[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (03): : 341 - 343
[5] THE DEL(4) (Q31) SYNDROME - A RECOGNIZABLE DISORDER WITH ATYPICAL ROBIN MALFORMATION SEQUENCE - BRIEF CLINICAL REPORT
DAVIS, JM
CLARREN, SK
SALK, DJ
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (02): : 113 - 117
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