CLINICAL AND CYTOGENETIC STUDIES OF 2 INFANTS WITH PARTIAL MONOSOMY-G

被引：12

作者：

MAEDA, T

OHNO, M

NISHIDA, H

机构：

[1] KITASATO UNIV,SCH MED,DEPT LAB MED,SAGAMIHARA,KANAGAWA,JAPAN

[2] KITASATO UNIV,SCH MED,DEPT PEDIAT,SAGAMIHARA,KANAGAWA,JAPAN

来源：

HUMAN GENETICS | 1977年 / 35卷 / 03期

关键词：

D O I：

10.1007/BF00446618

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：255 / 259

页数：5

共 15 条

[1]

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[8]

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[9] KARYOTYPE 45,XX,-21/46,XX,21Q IN AN INFANT WITH SYMPTOMS OF G-DELETION-SYNDROME-I [J].

MIKKELSEN, M ;

VESTERMARK, S .

JOURNAL OF MEDICAL GENETICS, 1974, 11 (04) :389-393

[10] G DELETION SYNDROME ANTI-MONGOLISM [J].

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