The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

标题
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
作者
关键词
-
出版物
JOURNAL OF MEDICAL GENETICS
Volume 48, Issue 6, Pages 396-406
出版商
BMJ
发表日期
2011-03-26
DOI
10.1136/jmg.2010.087528

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