Disease: Craniometaphyseal dysplasia- autosomal dominant
- A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia
- A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)
- A three-year clinical investigation of a Chinese child with craniometaphyseal dysplasia caused by a mutated <em>ANKH</em> gene
- An atypical case of craniometaphyseal dysplasia. Case report and surgical treatment
- Associations of polygenic inheritance of physical activity with aerobic fitness, cardiometabolic risk factors and diseases: the HUNT study
- Cochlear Implantation in Craniometaphyseal Dysplasia
- Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locus
- Craniometaphyseal Dysplasia, Autosomal Dominant
- Craniometaphyseal dysplasia: a case report
- Craniometaphyseal dysplasia: Report of 2 cases with an emphasis on panoramic imaging features
- Foramen magnum decompression and expansile duroplasty for acquired Chiari type I malformation in craniometaphyseal dysplasia
- Induced pluripotent stem cell reprogramming by integration-free Sendai virus vectors from peripheral blood of patients with craniometaphyseal dysplasia
- Introduction of a Phe377del mutation in ANK creates a mouse model for craniometaphyseal dysplasia
- Localization of the gene for hyperostosis cranialis interna to chromosome 8p21 with analysis of three candidate genes
- Restriction of Dietary Phosphate Ameliorates Skeletal Abnormalities in a Mouse Model for Craniometaphyseal Dysplasia
- The kynurenine pathway in major depressive disorder under different disease states: A systematic review and meta-analysis