Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability.
about
Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts.Meis2 is essential for cranial and cardiac neural crest developmentDe novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux.A 15q14 microdeletion involving MEIS2 identified in a patient with autism spectrum disorder.Identification of novel candidate disease genes from de novo exonic copy number variants.Monogenic disorders that mimic the phenotype of Rett syndrome.Face morphogenesis is promoted by Pbx-dependent EMT via regulation of Snail1 during frontonasal prominence fusion.A commentary on de novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux.Quantification of Phenotype Information Aids the Identification of Novel Disease Genes.
P2860
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P2860
Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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name
Haploinsufficiency of MEIS2 is ...... fting and learning disability.
@en
Haploinsufficiency of MEIS2 is ...... fting and learning disability.
@nl
type
label
Haploinsufficiency of MEIS2 is ...... fting and learning disability.
@en
Haploinsufficiency of MEIS2 is ...... fting and learning disability.
@nl
prefLabel
Haploinsufficiency of MEIS2 is ...... fting and learning disability.
@en
Haploinsufficiency of MEIS2 is ...... fting and learning disability.
@nl
P2093
P2860
P50
P356
P1476
Haploinsufficiency of MEIS2 is ...... fting and learning disability.
@en
P2093
Atle Brendehaug
Ernie Bongers
Gunnar Helland
Gunnar Houge
Gyri Aasland Gradek
Madeleine Fannemel
Nicole de Leeuw
Olaug Rødningen
Randi Hovland
Rolph Pfundt
P2860
P304
P356
10.1002/AJMG.A.36498
P407
P577
2014-03-26T00:00:00Z