DE1(3)(P25.3) WITHOUT PHENOTYPIC EFFECT

被引：43

作者：

KNIGHT, LA

YONG, MH

TAN, M

NG, ISL

机构：

[1] SINGAPORE GEN HOSP,DEPT PATHOL,SINGAPORE 0316,SINGAPORE

[2] SINGAPORE GEN HOSP,DEPT PAEDIAT,SINGAPORE 0316,SINGAPORE

来源：

JOURNAL OF MEDICAL GENETICS | 1995年 / 32卷 / 12期

关键词：

D O I：

10.1136/jmg.32.12.994

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for the 3p- syndrome. A normal baby girl was born with no apparant phenotypic abnormalities.

引用

页码：994 / 995

页数：2

共 4 条

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[2]

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