Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing-Reference-Cited by-同舟云学术

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Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing

Published:2017-01 Issue:1 Volume:16 Page:473-477
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

Deng Hao,Tan Ting,He Quanyong,Lin Qiongfen,Yang Zhijian,Zhu Anding,Guan Liping,Xiao Jingjing,Song Zhi,Guo Yi

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families;Genetics in Medicine;2023-11

2. A novel Hoxd13 mutation causes synpolydactyly and promotes osteoclast differentiation by regulating pSmad5/p65/c-Fos/Rank axis;Cell Death & Disease;2023-02-20

3. A novel HOXD13 mutation causes synpolydactyly and promotes osteoclast differentiation by regulating pSMAD5/p65/c-Fos/RANK axis;2022-11-28

4. Identification of a HOXD13 variant in a Mongolian family with incomplete penetrance syndactyly by exon sequencing;BMC Medical Genomics;2022-10-04

5. Recent Advances in Syndactyly: Basis, Current Status and Future Perspectives;Genes;2022-04-27

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