Associated Papers
New insight into the development of synpolydactyly caused by expansion of HOXD13 polyalanine based on weighted gene co-expression network analysis.
Chen X et al.
Bmc Medical Genomics, 2024
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
Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families.
Zu B et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists, 2021
A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family.
Zaib T et al.
Bmc Medical Genetics, 2019
[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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