Associated Papers
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
Anorectal and urinary anomalies and aberrant retinoic acid metabolism in cytochrome P450 oxidoreductase deficiency.
Fukami M et al.
Molecular Genetics and Metabolism, 2010
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