CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
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DeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing dataEFTUD2 deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish model.Crim1 regulates integrin signaling in murine lens development.Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma.Evaluation of individual aging degree by standard-free, label-free LC-MS/MS quantification of formaldehyde-modified peptides.Application of Whole Genome Sequencing Technology in the Investigation of Genetic Causes of Fetal, Perinatal, and Early Infant Death.
P2860
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
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2015 nî lūn-bûn
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2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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name
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
@ast
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
@en
type
label
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
@ast
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
@en
prefLabel
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
@ast
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
@en
P2093
P2860
P356
P1476
CRIM1 haploinsufficiency causes defects in eye development in human and mouse.
@en
P2093
Bernd Wollnik
Ebru Toker
Filippo Beleggia
Irene H Maumenee
Jieqing Fan
Nursel H Elcioğlu
Richard Lang
Thomas Wieland
Tim M Strom
P2860
P304
P356
10.1093/HMG/DDU744
P577
2015-01-05T00:00:00Z