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Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensitiesTALEN-based generation of a cynomolgus monkey disease model for human microcephaly.The DNA damage response molecule MCPH1 in brain development and beyond.Genetic heterogeneity in Pakistani microcephaly families revisited.
P2860
description
2015 nî lūn-bûn
@nan
2015 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի մարտին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
MCPH1: a window into brain development and evolution.
@ast
MCPH1: a window into brain development and evolution.
@en
type
label
MCPH1: a window into brain development and evolution.
@ast
MCPH1: a window into brain development and evolution.
@en
prefLabel
MCPH1: a window into brain development and evolution.
@ast
MCPH1: a window into brain development and evolution.
@en
P2093
P2860
P356
P1476
MCPH1: a window into brain development and evolution.
@en
P2093
Jeannette Nardelli
Jeremy N Pulvers
P2860
P356
10.3389/FNCEL.2015.00092
P577
2015-03-27T00:00:00Z