A NEW CASE OF PROXIMAL 10Q PARTIAL TRISOMY

被引:11
作者
DEMICHELENA, MI
CAMPOS, PJ
机构
[1] UNIV PERUANA CAYETANO HEREDIA,DEPT MORPHOL SCI,LIMA,PERU
[2] UNIV PERUANA CAYETANO HEREDIA,DEPT PEDIAT,LIMA,PERU
关键词
D O I
10.1136/jmg.28.3.205
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a girl with mild phenotypic abnormalities and duplication of chromosome 10q11 --> 10q22. The similarities to two previously reported cases with an identical chromosomal aberration provide further support for the delineation of this entity as a specific, clinically recognisable syndrome.
引用
收藏
页码:205 / 206
页数:2
相关论文
共 2 条
[1]  
FRYNS JP, 1987, CLIN GENET, V32, P61
[2]  
VOGEL W, 1978, CLIN GENET, V13, P159