A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation

Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families

(2014) Limeng Dai et al.   PLoS One

Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome

(2014) T. Zemojtel et al.   Science Translational Medicine

Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A

(2013) Pia Kuss et al.   DEVELOPMENTAL BIOLOGY

Joining the fingers: AHOXD13story

(2013) Nathalie Brison et al.   DEVELOPMENTAL DYNAMICS

Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutations

(2013) D. M. Ibrahim et al.   GENOME RESEARCH

A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance

(2011) Mazen Kurban et al.   JOURNAL OF HUMAN GENETICS

Homeobox genes d11–d13 and a13 control mouse autopod cortical bone and joint formation

(2010) Pablo Villavicencio-Lorini et al.   JOURNAL OF CLINICAL INVESTIGATION

The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease

(2008) Peter N. Robinson et al.   AMERICAN JOURNAL OF HUMAN GENETICS