OCULODENTODIGITAL DYSPLASIA AND TYPE-III SYNDACTYLY - SEPARATE GENETIC ENTITIES OR DISEASE SPECTRUM

被引：21

作者：

BRUETON, LA

HUSON, SM

FARREN, B

WINTER, RM

机构：

[1] Kennedy Galton Centre, Clinical Research Centre, Northwick Park Hospital, Harrow, Middlesex HA1 3UJ, Watford Road

来源：

JOURNAL OF MEDICAL GENETICS | 1990年 / 27卷 / 03期

关键词：

D O I：

10.1136/jmg.27.3.169

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A family is described with type III syndactyly and facies resembling the oculodentodigital dysplasia facial phenotype in the absence of any of the other characteristic findings of the latter condition. The relationship between type III syndactyly and oculodentodigital dysplasia is discussed.

引用

页码：169 / 175

页数：7

共 13 条

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