Human Genome Epidemiology Literature Finder
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Query Trace: Hypertelorism 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 |
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- Page last updated:Apr 22, 2024
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