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Quoted phrase not found in phrase index: "Craniosynostosis and dental anomalies"
Page 1
Dental approach for Apert syndrome in children: a systematic review.
Med Oral Patol Oral Cir Bucal. 2017 Nov 1;22(6):e660-e668. doi: 10.4317/medoral.21628.
Med Oral Patol Oral Cir Bucal. 2017.
PMID: 29053644
Free PMC article.
Review.
BACKGROUND: Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from missense mutations in the gene encoding fibroblast growth factor receptor 2. It is characterized by three specific clinical features: brachycep …
BACKGROUND: Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from mis …
Le Fort III distraction osteogenesis versus conventional Le Fort III osteotomy in correction of syndromic midfacial hypoplasia: a systematic review.
Saltaji H, Altalibi M, Major MP, Al-Nuaimi MH, Tabbaa S, Major PW, Flores-Mir C.
Saltaji H, et al.
J Oral Maxillofac Surg. 2014 May;72(5):959-72. doi: 10.1016/j.joms.2013.09.039. Epub 2013 Oct 9.
J Oral Maxillofac Surg. 2014.
PMID: 24280172
Review.
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