Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Archivum Immunologiae Et Therapiae Experimentalis|December 4, 2004
The search for a genetic defect in Polish patients with chronic granulomatous diseaseMonika Jurkowska, Magdalena Kurenko-Deptuch, Jerzy Bal, et al.
Medycyna Wieku Rozwojowego|October 20, 2009
[Angelman syndrome--the research model of epigenetic mechanisms expression genes regulation]Agnieszka Szpecht-Potocka, Monika Gos, Radosław Struniawski, et al.
Developmental Period Medicine|March 17, 2016
Genetic analysis in inherited metabolic disorders--from diagnosis to treatment. Own experience, current state of knowledge and perspectivesKatarzyna Wertheim-Tysarowska, Monika Gos, Jolanta Sykut-Cegielska, et al.
European Journal of Cell Biology|March 17, 2015
Complex interplay between the length and composition of the huntingtin-derived peptides modulates the intracellular behavior of the N-terminal fragments of mutant huntingtinMichał Milewski, Paweł Gawliński, Daniel Bąk, et al.
Brain & Development|December 19, 2012
Mutations in the PLP1 gene residue p. Gly198 as the molecular basis of Pelizeaus-Merzbacher phenotypeDorota Hoffman-Zacharska, Tomasz Kmieć, Jarosław Poznański, et al.
Medycyna Wieku Rozwojowego|October 20, 2009
[Analysis of genomic imprinting defects in Angelman syndrome with application of quantitative real-time PCR]Agnieszka Szpecht-Potocka, Monika Gos, Radosław Struniawski, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|December 10, 2014
Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial CleftingAgnieszka Charzewska, Ewa Obersztyn, Dorota Hoffman-Zacharska, et al.
Medycyna Wieku Rozwojowego|June 14, 2005
[Prenatal diagnosis of cystic fibrosis in risk families in Poland--results of molecular analysis]Jerzy Bal, Agnieszka Sobczyńska-Tomaszewska, Kamila Czerska, et al.
Neurologia I Neurochirurgia Polska|August 30, 2014
Intrafamilial variability of the primary dystonia DYT6 phenotype caused by p.Cys5Trp mutation in THAP1 geneMarta Jurek, Dorota Hoffman-Zacharska, Dariusz Koziorowski, et al.
Pediatric Neurology|July 11, 2009
A family with paroxysmal nonkinesigenic dyskinesia: genetic and treatment issuesKrzysztof Szczałuba, Marta Jurek, Elzbieta Szczepanik, et al.
Pageof 8