Associated Papers
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
[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
Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly.
Gong L et al.
European Journal of Medical Genetics, 0
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