标题
Identification ofC12orf4as a gene for autosomal recessive intellectual disability
作者
关键词
-
出版物
CLINICAL GENETICS
Volume 91, Issue 1, Pages 100-105
出版商
Wiley
发表日期
2016-06-17
DOI
10.1111/cge.12821
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules
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- The Finnish Disease Heritage Database (FinDis) Update-A Database for the Genes Mutated in the Finnish Disease Heritage Brought to the Next-Generation Sequencing Era
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- Genetic and Epigenetic Networks in Intellectual Disabilities
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- Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome
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