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Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.

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Bibliographic Details
Title: Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.
Authors: Kumar, Umesh1 (AUTHOR) umeshchandolia@rediffmail.com, Ray, Saugat2 (AUTHOR), Thapa, Amrit2 (AUTHOR), Walia, Baljinder Singh2 (AUTHOR), Chakrabarty, Barun Kumar3 (AUTHOR)
Source: Journal of Genetics. Jun2026, Vol. 105 Issue 1, p1-7. 7p.
Database: Academic Search Ultimate
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Description
ISSN:00221333
DOI:10.1007/s12041-026-01527-2