Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
about
Epidemiology, Etiology, and Treatment of Isolated Cleft PalatePalatogenesis and cutaneous repair: A two-headed coinDevelopments in our understanding of the genetic basis of birth defectsNew insights into craniofacial malformationsHeterozygous deletion of ventral anterior homeobox (vax1) causes subfertility in miceImputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan AfricaTGFA and IRF6 contribute to the risk of nonsyndromic cleft lip with or without cleft palate in northeast ChinaConditioning adaptive combination of P-values method to analyze case-parent trios with or without population controls.Pax7 is regulated by cMyb during early neural crest development through a novel enhancerA multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.Genetics of cleft lip and cleft palate.Disrupting hedgehog and WNT signaling interactions promotes cleft lip pathogenesis.Genomic approaches for studying craniofacial disorders.Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations.Genetics and genomics etiology of nonsyndromic orofacial clefts.Vax1 Plays an Indirect Role in the Etiology of Murine Cleft Palate.Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians.Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population.Medical genetics and genomic medicine in Nigeria.
P2860
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P2860
Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
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2013年學術文章
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name
Replication of genome wide ass ...... he etiology of nonsyndromic CL
@nl
Replication of genome wide ass ...... tiology of nonsyndromic CL(P).
@en
type
label
Replication of genome wide ass ...... he etiology of nonsyndromic CL
@nl
Replication of genome wide ass ...... tiology of nonsyndromic CL(P).
@en
prefLabel
Replication of genome wide ass ...... he etiology of nonsyndromic CL
@nl
Replication of genome wide ass ...... tiology of nonsyndromic CL(P).
@en
P2093
P2860
P356
P1476
Replication of genome wide ass ...... etiology of nonsyndromic CL(P)
@en
P2093
Adela M Mansilla
Aline L Petrin
Azeez Butali
Gongorjav Ayanga
Hideto Imura
Hiroo Furukawa
Jeffery C Murray
Karen Cuenco
Kumiko Fujiwawa
Margaret E Cooper
P2860
P304
P356
10.1002/AJMG.A.35749
P407
P577
2013-03-05T00:00:00Z