A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1

标题
A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1
作者
关键词
-
出版物
GENE
Volume 538, Issue 1, Pages 30-35
出版商
Elsevier BV
发表日期
2014-01-17
DOI
10.1016/j.gene.2014.01.027

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