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   Bailing Zu et al, 2021, Developmental Dynamics CrossRef
2. Identification of a GNE homozygous mutation in a Han‐Chinese family with GNE myopathy
   Yuan Wu et al, 2018, Journal of Cellular and Molecular Medicine CrossRef
3. Novel HOXD13 variants in syndactyly type 1b and type 1c, and a new spectrum of TP63-related disorders
   Rashmi Patel et al, 2022, Journal of Human Genetics CrossRef
4. Recent Advances in Syndactyly: Basis, Current Status and Future Perspectives
   Tahir Zaib et al, 2022, Genes CrossRef
5. Context-dependent HOX transcription factor function in health and disease
   Sarah E. Bondos et al, 2020, Dancing Protein Clouds: Intrinsically Disordered Proteins in Health and Disease, Part B CrossRef
6. Identification of a HOXD13 variant in a Mongolian family with incomplete penetrance syndactyly by exon sequencing
   Husile Husile et al, 2022, BMC Medical Genomics CrossRef
7. Novel GLI3 Mutations in Chinese Patients with Non-syndromic Post-axial Polydactyly
   X. Chen et al, 2019, Current Molecular Medicine CrossRef
8. HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families
   Annika Gottschalk et al, 2023, Genetics in Medicine CrossRef
9. A novel Hoxd13 mutation causes synpolydactyly and promotes osteoclast differentiation by regulating pSmad5/p65/c-Fos/Rank axis
   Lishan Zhang et al, 2023, Cell Death & Disease CrossRef
10. Identification of novel missense mutations associated with non-syndromic syndactyly in two vietnamese trios by whole exome sequencing
    Nguyen Thy Ngoc et al, 2020, Clinica Chimica Acta CrossRef