Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Yu-Peng Liu, Yu-Ling Kuo, Yen-Ni Chen, . . . Wayseen Wang. (2014). Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome. Elsevier.
Chicago Style (17th ed.) CitationChih-Ping Chen, et al. Prenatal Diagnosis and Molecular Cytogenetic Characterization of a 1.07-Mb Microdeletion at 5q35.2-q35.3 Associated with NSD1 Haploinsufficiency and Sotos Syndrome. Elsevier, 2014.
MLA (9th ed.) CitationChih-Ping Chen, et al. Prenatal Diagnosis and Molecular Cytogenetic Characterization of a 1.07-Mb Microdeletion at 5q35.2-q35.3 Associated with NSD1 Haploinsufficiency and Sotos Syndrome. Elsevier, 2014.
Warning: These citations may not always be 100% accurate.