三体
比较基因组杂交
基因复制
生物
胼胝体发育不全
微缺失综合征
遗传学
胼胝体
染色体
解剖
基因
作者
Deniz Karçaaltıncaba,Serdar Ceylaner,Gülay Ceylaner,Semih Dalkılıç,Kader Karlı-Oğuz,Ömer Kandemir
出处
期刊:PubMed
日期:2010-01-01
卷期号:21 (1): 19-24
被引量:8
摘要
We report a case of partial trisomy 22q with de novo duplication of chromosomal region 22q11.1-22q13.1, also confirmed by microarray comparative genomic hybridization (Array-CGH) analysis. The fetus had interhemispheric cyst and corpus callosum agenesis diagnosed by MRI which has not been reported in the literature. This novel phenotype differs from the reported cat eye syndromes by the absence of heart defects and the presence of brain anomalies.
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