换一批
换一批Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.
作者：
主题词
成年人(Adult);儿童, 学龄前(Child, Preschool);染色体, 人, 14对(Chromosomes, Human, Pair 14);比较基因组杂交(Comparative Genomic Hybridization);发育障碍(Developmental Disabilities);癫痫(Epilepsy);女(雌)性(Female);叉头转录因子类(Forkhead Transcription Factors);基因复制(Gene Duplication);人类(Humans);婴儿(Infant);语言发展障碍(Language Development Disorders);男(雄)性(Male);神经组织蛋白质类(Nerve Tissue Proteins);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis)
DOI
10.1038/ejhg.2010.142
PMID
20736978
发布时间
2021-10-28
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