A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
about
Language Impairments in ASD Resulting from a Failed Domestication of the Human BrainMutations in WNT10B Are Identified in Individuals with OligodontiaExpanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis.
P2860
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
@ast
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
@en
type
label
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
@ast
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
@en
prefLabel
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
@ast
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
@en
P2093
P2860
P1433
P1476
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.
@en
P2093
Hailan Feng
Haochen Liu
Tingting Ding
P2860
P304
P356
10.1371/JOURNAL.PONE.0138221
P407
P577
2015-09-25T00:00:00Z