Associated Papers
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
Joining the fingers: a HOXD13 Story.
Brison N et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists, 2014
Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.
Dai L et al.
Plos One, 2014
Isolated brachydactyly type E caused by a HOXD13 nonsense mutation: a case report.
Jamsheer A et al.
Bmc Medical Genetics, 2012
Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery.
Furniss D et al.
Journal of Medical Genetics, 2009
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