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Archiwum Medycyny Sadowej I Kryminologii|October 4, 2017
Application of massively parallel sequencing (MPS) in paternity testing - case reportGrażyna Kostrzewa, Magdalena Konarzewska, Witold Pepiński
Plos One|August 13, 2013
Genetic polymorphism of human Y chromosome and risk factors for cardiovascular diseases: a study in WOBASZ cohortGrażyna Kostrzewa, Grażyna Broda, Magdalena Konarzewska, et al.
American Journal of Medical Genetics. Part A|August 27, 2021
A recurrent de novo variant supports KCNC2 involvement in the pathogenesis of developmental and epileptic encephalopathyMałgorzata Rydzanicz, Piotr Zwoliński, Piotr Gasperowicz, et al.
Journal of Applied Genetics|October 20, 2017
Mild Zellweger syndrome due to a novel PEX6 mutation: correlation between clinical phenotype and in silico prediction of variant pathogenicityMałgorzata Rydzanicz, Teresa Joanna Stradomska, Elżbieta Jurkiewicz, et al.
American Journal of Medical Genetics. Part A|February 3, 2022
Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosisMałgorzata Rydzanicz, Wojciech Glinkowski, Anna Walczak, et al.
Seizure|August 15, 2024
The epilepsy phenotype of KCNK4-related neurodevelopmental diseaseMagdalena Krygier, Szymon Ziętkiewicz, Weronika Talaśka-Liczbik, et al.
Cardiology|October 7, 2010
Cytochrome P450 2C19 polymorphism, suboptimal reperfusion and all-cause mortality in patients with acute myocardial infarctionLukasz A Małek, Jakub Przyłuski, Mateusz Spiewak, et al.
American Journal of Medical Genetics. Part A|June 16, 2025
The Attenuated Phenotype of CNTNAP1-Related Neuropathy Mimics Spastic-Dystonic Cerebral PalsyMagdalena Krygier, Michael Zech, Magdalena Chylińska, et al.
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