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Quoted phrase not found in phrase index: "Hypoplasia of mandible relative to maxilla"
Page 1
Molecular Basis for Craniofacial Phenotypes Caused by Sclerostin Deletion.
Chen J, Yuan X, Pilawski I, Liu X, Delgado-Calle J, Bellido T, Turkkahraman H, Helms JA. Chen J, et al. J Dent Res. 2021 Mar;100(3):310-317. doi: 10.1177/0022034520963584. Epub 2020 Oct 20. J Dent Res. 2021. PMID: 33078679 Free PMC article.
Affected patients have a high bone mass coupled with a distinctive appearance where the mandible is enlarged and the maxilla is foreshortened. Here, mice carrying a null mutation in Sost were analyzed using quantitative micro-computed tomographic (CT) imaging and hi …
Affected patients have a high bone mass coupled with a distinctive appearance where the mandible is enlarged and the maxilla i …
Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes.
Kantaputra PN, Tripuwabhrut K, Intachai W, Carlson BM, Quarto N, Ngamphiw C, Tongsima S, Sonsuwan N. Kantaputra PN, et al. Clin Otolaryngol. 2020 Sep;45(5):695-702. doi: 10.1111/coa.13560. Epub 2020 May 25. Clin Otolaryngol. 2020. PMID: 32351010 Free article.
OBJECTIVE: To investigate four Treacher Collins syndrome patients of the Sgaw Karen family living in Thailand. METHOD: Clinical examination, hearing tests, lateral cephalometric analyses, Computed tomography, whole exome sequencing and Sanger direct sequencing were perform …
OBJECTIVE: To investigate four Treacher Collins syndrome patients of the Sgaw Karen family living in Thailand. METHOD: Clinical exami …
Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.
Clauss F, Waltmann E, Barriere P, Hadj-Rabia S, Manière MC, Schmittbuhl M. Clauss F, et al. J Craniomaxillofac Surg. 2014 Sep;42(6):e346-51. doi: 10.1016/j.jcms.2014.01.037. Epub 2014 Jan 15. J Craniomaxillofac Surg. 2014. PMID: 24702986 Review.
PURPOSE: To report the dento-craniofacial phenotype of a family affected by a WNT10A HED and to describe the implant-based oral rehabilitation of a patient presenting a severe oligodontia linked to this mutation. ...RESULTS: Severe oligodontia was observed in the patient a …
PURPOSE: To report the dento-craniofacial phenotype of a family affected by a WNT10A HED and to describe the implant-based oral rehab …
Tooth agenesis and craniofacial morphology in an orthodontic population.
Tavajohi-Kermani H, Kapur R, Sciote JJ. Tavajohi-Kermani H, et al. Am J Orthod Dentofacial Orthop. 2002 Jul;122(1):39-47. doi: 10.1067/mod.2002.123948. Am J Orthod Dentofacial Orthop. 2002. PMID: 12142896
Area measurements of the jaw size of the subjects grouped by age were compared with Bolton cephalometric templates. Relatively little correlation was found between missing teeth and changes in cephalometric measurements. ...Two-dimensional area measurements showed that mos …
Area measurements of the jaw size of the subjects grouped by age were compared with Bolton cephalometric templates. Relatively little …