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Medycyna Wieku Rozwojowego|February 5, 2013
Assessment of the role of copy-number variants in 150 patients with congenital heart defectsKatarzyna Derwińska, Magdalena Bartnik, Barbara Wiśniowiecka-Kowalnik, et al.Journal of Applied Genetics|December 4, 2013
Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disabilityMagdalena Bartnik, Beata Nowakowska, Katarzyna Derwińska, et al.European Urology|March 19, 2016
Gene Expression Profile of the Clinically Aggressive Micropapillary Variant of Bladder CancerCharles Chuanhai Guo, Vipulkumar Dadhania, Li Zhang, et al.Journal of Medical Genetics|October 25, 2018
Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to <i>EFNA5</i>, <i>BAHD1</i> and <i>PPP2R5E</i> as novel candidates for genes causing human Mendelian disordersVictor Murcia Pienkowski, Marzena Kucharczyk, Marlena Młynek, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 25, 2012
Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disordersMagdalena Bartnik, Elżbieta Szczepanik, Katarzyna Derwińska, et al.Human Mutation|September 18, 2010
Detection of clinically relevant exonic copy-number changes by array CGHPhilip M Boone, Carlos A Bacino, Chad A Shaw, et al.Pageof 2