A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.
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Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese familiesFunctional classification and mutation analysis of a synpolydactyly kindred.Advances in the Molecular Genetics of Non-syndromic Syndactyly.Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.
P2860
A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.
description
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
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2012年学术文章
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2012年學術文章
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name
A novel non-synonymous mutatio ...... lydactyly in a Chinese family.
@en
A novel non-synonymous mutatio ...... lydactyly in a Chinese family.
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type
label
A novel non-synonymous mutatio ...... lydactyly in a Chinese family.
@en
A novel non-synonymous mutatio ...... lydactyly in a Chinese family.
@nl
prefLabel
A novel non-synonymous mutatio ...... lydactyly in a Chinese family.
@en
A novel non-synonymous mutatio ...... lydactyly in a Chinese family.
@nl
P2093
P1433
P1476
A novel non-synonymous mutatio ...... lydactyly in a Chinese family.
@en
P2093
Baoqiang Xu
Binbin Wang
Guang Yang
Longfei Cheng
P304
P356
10.1016/J.CCA.2012.02.015
P50
P577
2012-02-22T00:00:00Z