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Article

A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance

4 Aug 2011

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 21814222
DOI: 10.1038/jhg.2011.84

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Related research

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Research trail→

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A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrancePMID 21814222Read ↗

Homozygous nonsense mutation in HOXD13 underlies synpolydactyly with a cleft.Semantic proximity Read ↗

HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families.Semantic proximity Read ↗

A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family.Semantic proximity Read ↗

Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.Semantic proximity Read ↗

Joining the fingers: a HOXD13 Story.Semantic proximity Read ↗

A novel mutation outside homeodomain of HOXD13 causes synpolydactyly in a Chinese family.Semantic proximity Read ↗

Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly.Semantic proximity Read ↗

Mutation analysis of HOXD13 gene in a Chinese pedigree with synpolydactyly.Semantic proximity Read ↗

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.Semantic proximity Read ↗

Limb skeletal malformations - what the HOX is going on?Semantic proximity Read ↗

Long-Read Whole-Genome Sequencing Uncovers a Deletion Upstream to HOXD13 Causing Synpolydactyly.Semantic proximity Read ↗

A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.Semantic proximity Read ↗

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