Craniofacial morphology in patients with hypophosphatemic rickets: A cephalometric study focusing on differences between bone of cartilaginous and intramembranous origin
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34242/fullpdf
Reference32 articles.
1. Craniofacial morphology in patients with hypophosphataemic vitamin-D-resistant rickets: A cephalometric study;Al-Jundi;J Oral Rehabil,2009
2. Longitudinal cephalometric standards for the neurocranium in Norwegians from 6 to 21 years of age;Axelsson;Eur J Orthod,2003
3. Prevalence and pathogenesis of dental and periodontal lesions in children with X-linked hypophosphatemic rickets;Baroncelli;Eur J Paediatr Dent,2006
4. Incidence and prevalence of nutritional and hereditary rickets in southern Denmark;Beck-Nielsen;Eur J Endocrinol,2009
5. Phenotype presentation of hypophosphatemic rickets in adults;Beck-Nielsen;Calcif Tissue Int,2010
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1. Orthodontic treatment in children and adolescent patients with X‐linked hypophosphatemia: A case–control study;Orthodontics & Craniofacial Research;2024-04-12
2. Craniofacial morphology in adults with osteogenesis imperfecta—A cross‐sectional study;Orthodontics & Craniofacial Research;2022-09-08
3. Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium;Frontiers in Endocrinology;2021-03-19
4. Oral health‐related quality of life in X‐linked hypophosphataemia and osteogenesis imperfecta;Journal of Oral Rehabilitation;2020-11-19
5. Mineralized tissues in hypophosphatemic rickets;Pediatric Nephrology;2019-08-08
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