APA (7th ed.) Citation

Kumar, U., Ray, S., Thapa, A., Walia, B. S., & Chakrabarty, B. K. (2026). Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report. Journal of Genetics, 105(1), 1. https://doi.org/10.1007/s12041-026-01527-2

Chicago Style (17th ed.) Citation

Kumar, Umesh, Saugat Ray, Amrit Thapa, Baljinder Singh Walia, and Barun Kumar Chakrabarty. "Craniometaphyseal Dysplasia with Severe Maxillary Hypoplasia Due to ANKH Gene Mutation: A Case Report." Journal of Genetics 105, no. 1 (2026): 1. https://doi.org/10.1007/s12041-026-01527-2.

MLA (9th ed.) Citation

Kumar, Umesh, et al. "Craniometaphyseal Dysplasia with Severe Maxillary Hypoplasia Due to ANKH Gene Mutation: A Case Report." Journal of Genetics, vol. 105, no. 1, 2026, p. 1, https://doi.org/10.1007/s12041-026-01527-2.