Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Otitis Media and FGFR2[original query] |
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Mutations in the FGFR2 gene in Mexican patients with Apert syndrome. Genetics and molecular research : GMR 2015 14 (1): 2341-6. Ibarra-Arce A, Ortiz de Zárate-Alarcón G, Flores-Peña L G, Martínez-Hernández F, Romero-Valdovinos M, Olivo-Díaz |
Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation. The Journal of craniofacial surgery 2021 Jul . Kilcoyne Sarah, Luscombe Carrie, Scully Paula, Overton Sarah, Brockbank Sally, Swan Marc C, Johnson David, Wall Steven, Wilkie Andrew O |
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- Page last updated:Apr 29, 2024
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