A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
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Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunitiesImputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population.Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and MiceGenome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.Zebrafish models of orofacial clefts.IRF6 and SPRY4 Signaling Interact in Periderm Development.The Role of Noncoding Genetic Variation in Isolated Orofacial Clefts.Grainyhead-like Transcription Factors in Craniofacial Development.Rare deleterious variants in GRHL3 are associated with human spina bifida.Genetic Interactions in Nonsyndromic Orofacial Clefts in Europe-EUROCRAN Study.Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing.Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate.A Population-Based Study of Effects of Genetic Loci on Orofacial Clefts.Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.Genetics and genomics etiology of nonsyndromic orofacial clefts.Mis-expression of grainyhead-like transcription factors in zebrafish leads to defects in enveloping layer (EVL) integrity, cellular morphogenesis and axial extension.Structural basis of gene regulation by the Grainyhead/CP2 transcription factor family.Association of MEOX2 polymorphism with nonsyndromic cleft palate only in a Vietnamese population.Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2.Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate.Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.Craniofacial genetics: Where have we been and where are we going?Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation
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P2860
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
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2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
A Genome-wide Association Stud ...... gic Missense Variant in GRHL3.
@ast
A Genome-wide Association Stud ...... gic Missense Variant in GRHL3.
@en
type
label
A Genome-wide Association Stud ...... gic Missense Variant in GRHL3.
@ast
A Genome-wide Association Stud ...... gic Missense Variant in GRHL3.
@en
prefLabel
A Genome-wide Association Stud ...... gic Missense Variant in GRHL3.
@ast
A Genome-wide Association Stud ...... gic Missense Variant in GRHL3.
@en
P2093
P2860
P50
P1476
A Genome-wide Association Stud ...... gic Missense Variant in GRHL3.
@en
P2093
Alexandre R Vieira
Ana Maria Lopez-Palacio
Andrew C Lidral
Andrew E Czeizel
Azeez Butali
Babatunde S Aregbesola
Beth Emanuele
Carla Sanchez
Carmen J Buxó
Carmencita D Padilla
P2860
P304
P356
10.1016/J.AJHG.2016.02.014
P407
P50
P577
2016-03-22T00:00:00Z