CHROMOSOME-ABNORMALITIES AND WILLIAMS SYNDROME

被引：8

作者：

GREENBERG, F

LEDBETTER, DH

机构：

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 30卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320300423

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：993 / 994

页数：2

共 6 条

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[2]

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

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DAVISON, EV .

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[4] CLINICAL HETEROGENEITY ASSOCIATED WITH DELETIONS IN THE LONG ARM OF CHROMOSOME-15 - REPORT OF 3 NEW CASES AND THEIR POSSIBLE GENETIC SIGNIFICANCE [J].

KAPLAN, LC ;

WHARTON, R ;

ELIAS, E ;

MANDELL, F ;

DONLON, T ;

LATT, SA .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (01) :45-53

[5] IDIOPATHIC INFANTILE HYPERCALCEMIA - A CONTINUING ENIGMA [J].

MARTIN, NDT ;

SNODGRASS, GJAI ;

COHEN, RD .

ARCHIVES OF DISEASE IN CHILDHOOD, 1984, 59 (07) :605-613

[6]

MILES JH, 1983, AM J HUM GENET, V35, pA144

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