ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

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Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations.

P2860

Q37649517-29F7F5D8-C4A9-4EBA-A2CA-8F22C9838DAF

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ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

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http://www.wikidata.org/entity/Q36062872

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

@zh-cn

2012年学术文章

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2012年学术文章

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2012年學術文章

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ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

@ast

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

@en

type

Item

label

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

@ast

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

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prefLabel

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

@ast

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

@en

P1476

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

@en

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Alan F Scott

http://www.w3.org/2001/XMLSchema#string

Ethylin Wang Jabs

http://www.w3.org/2001/XMLSchema#string

Felicia Sh Cheah

http://www.w3.org/2001/XMLSchema#string

Gerald V Raymond

http://www.w3.org/2001/XMLSchema#string

Hong Wang

http://www.w3.org/2001/XMLSchema#string

Ingo Ruczinski

http://www.w3.org/2001/XMLSchema#string

Jacqueline B Hetmanski

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Kung Yee Liang

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M Daniele Fallin

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Philip Kuo-Ting Chen

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P2860

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

PLINK: a tool set for whole-genome association and population-based linkage analyses

Contributions of PTCH gene variants to isolated cleft lip and palate

Haploview: analysis and visualization of LD and haplotype maps

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Robinow syndrome: phenotypic variability in a family with a novel intragenic ROR2 mutation

Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome

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476-480

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scholarly article

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English

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125

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2012-02-01T00:00:00Z

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22490406

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P932

3384720

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ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

about

P2860

P2860

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P407

P433

P478

P577

P698

P932

P1433

P1476

P2093

P2860

P304

P31

P407

P433

P478

P577

P698

P932