(2015). Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of apert syndrome.
Chicago Style (17th ed.) CitationMolecular Analysis of Exons 8, 9 and 10 of the Fibroblast Growth Factor Receptor 2 (FGFR2) Gene in Two Families with Index Cases of Apert Syndrome. 2015.
MLA (8th ed.) CitationMolecular Analysis of Exons 8, 9 and 10 of the Fibroblast Growth Factor Receptor 2 (FGFR2) Gene in Two Families with Index Cases of Apert Syndrome. 2015.
Warning: These citations may not always be 100% accurate.