INTERSTITIAL DELETION OF CHROMOSOME-18[DEL(18)(Q11.2Q12.2 OR Q12.2Q21.1]

被引：11

作者：

SURH, LC

LEDBETTER, DH

GREENBERG, F

机构：

[1] BAYLOR COLL MED,INST MOLEC GENET,1 BAYLOR PLAZA,HOUSTON,TX 77030

[2] BAYLOR COLL MED,DEPT BIOCHEM,HOUSTON,TX 77030

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 41卷 / 01期

关键词：

CHROMOSOME ABNORMALITY; CHROMOSOME-18;

D O I：

10.1002/ajmg.1320410105

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A 27-month-old boy with mild developmental delay, growth delay, strabismus, midface hypoplasia, relative telecanthus, downslanting palpebral fissures, epicanthal folds, dental hypoplasia, and cardiac defects was found to have an interstitial deletion of chromosome 18 involving band q12.1 or q12.3.

引用

页码：15 / 17

页数：3