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Quoted phrase not found in phrase index: "Osteogenesis imperfecta type 16"
Page 1
Dental anomalies in individuals with osteogenesis imperfecta: a systematic review and meta-analysis of prevalence and comparative studies.
Prado HV, Soares ECB, Carneiro NCR, Vilar ICO, Abreu LG, Borges-Oliveira AC. Prado HV, et al. J Appl Oral Sci. 2023 Sep 4;31:e20230040. doi: 10.1590/1678-7757-2023-0040. eCollection 2023. J Appl Oral Sci. 2023. PMID: 37672427 Free PMC article.
BACKGROUND: Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. ...Most prevalent dental anomalies in individuals with OI included pulp obliteration (46.4%), dental …
BACKGROUND: Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the …
A systematic review of genetic skeletal disorders reported in Chinese biomedical journals between 1978 and 2012.
Cui Y, Zhao H, Liu Z, Liu C, Luan J, Zhou X, Han J. Cui Y, et al. Orphanet J Rare Dis. 2012 Aug 22;7:55. doi: 10.1186/1750-1172-7-55. Orphanet J Rare Dis. 2012. PMID: 22913777 Free PMC article. Review.
This study systematically reviewed GSDs as defined in "Nosology and Classification of genetic skeletal disorders (2010 version)" using Chinese biomedical literature published over the past 34 years from 1978 to 2012. In total, 16,099 GSDs have been reported. The most frequ …
This study systematically reviewed GSDs as defined in "Nosology and Classification of genetic skeletal disorders (2010 version)" using Chine …