Associated Papers
Molecular Landscape in Limb Anomalies: Diagnostic Yield and New Candidate Genes.
Mokhtari A et al.
Clinical Genetics, 2026
Whole-genome sequencing identifies HOXD13 variants in syndactyly pedigrees.
Xu YF et al.
Human Genomics, 2025
HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families.
Gottschalk A et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2023
Clinical and genetic analysis in Chinese families with synpolydactyly, and cellular localization of HOXD13 with different length of polyalanine tract.
Chen X et al.
Frontiers in Genetics, 2023
Recent Advances in Syndactyly: Basis, Current Status and Future Perspectives.
Zaib T et al.
Genes, 2022
A Novel Missense Variant of HOXD13 Caused Atypical Synpolydactyly by Impairing the Downstream Gene Expression and Literature Review for Genotype-Phenotype Correlations.
Guo R et al.
Frontiers in Genetics, 2021
Advances in the Molecular Genetics of Non-syndromic Syndactyly.
Deng H et al.
Current Genomics, 2015
Functional classification and mutation analysis of a synpolydactyly kindred.
Zhou J et al.
Experimental and Therapeutic Medicine, 2014
[Synpolydactyly in a Chinese kindred: mutation detection, prenatal ultrasonographic and molecular diagnosis].
Jin H et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2011
Polyalanine repeat expansion mutations in the HOXD13 gene in Pakistani families with synpolydactyly.
Wajid M et al.
Clinical Genetics, 2009
[HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family].
Zhao XL et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2005
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