Associated Papers
Deciphering potential causative factors for undiagnosed Waardenburg syndrome through multi-data integration.
Sun F et al.
Orphanet Journal of Rare Diseases, 2024
38844942 (PubMed )
Supplement: 13023_2024_3220_MOESM8_ESM.xls › Sheet1
A novel missense mutation in the PAX3 gene in a case of Waardenburg syndrome type I.
Nakamura M et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2009
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