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Medicine

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

Umesh Kumar, S. Ray, A. Thapa, B. S. Walia, B. Chakrabarty

2026.4.7JOURNAL OF GENETICS

DOI: 10.1007/s12041-026-01527-2

Abstract

Abstract is not available.

Citation format

KUMAR, Umesh, et al. Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report. JOURNAL OF GENETICS, 2026, 105(1).