Associated Papers
Unraveling the Genetic Basis of Congenital Limb Anomalies in Eight Families.
Khan IU et al.
Clinical Genetics, 2025
Human HOX gene disorders.
Quinonez SC et al.
Molecular Genetics and Metabolism, 2014
Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.
Dai L et al.
Plos One, 2014
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