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Medycyna Wieku Rozwojowego|June 24, 2004
[I. Single nucleotide polymorphism in human genetic analyses]Kamila Czerska, Magdalena Nawara, Jerzy BalMedycyna Wieku Rozwojowego|June 14, 2005
[II. Pharmacogenetics--the future of modern pharmacology and genetics]Kamila Czerska, Jerzy BalMedycyna Wieku Rozwojowego|June 14, 2005
[Cystic fibrosis--a disease with many faces. The variable clinical picture versus the heterogeneity of molecular defect]Agnieszka Sobczynska-Tomaszewska, Kamila Czerska, Jerzy BalMedycyna Wieku Rozwojowego|June 18, 2003
[Monogenic causes of nonspecific X-linked mental retardation molecular aspects]Magdalena Nawara, Jerzy Bal, Tadeusz MazurczakMedycyna Wieku Rozwojowego|October 10, 2006
[Attention deficit hyperactivity disorder (ADHD)--molecular and genetic aspects]Anna Migdalska, Magdalena Nawara, Jerzy Bal, et al.Medycyna Wieku Rozwojowego|October 20, 2009
[Gene mapping in 14 families with X-linked nonspecific mental retardation]Magdalena Nawara, Marta Jurek, Jerzy Bal, 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.Medycyna Wieku Rozwojowego|April 6, 2011
[Genetic risk markers of low bone mineral density in cystic fibrosis children]Aleksandra Norek, Dorota Sands, Agnieszka Sobczyńska-Tomaszewska, et al.European Journal of Human Genetics : EJHG|August 16, 2012
Newborn screening for cystic fibrosis: Polish 4 years' experience with CFTR sequencing strategyAgnieszka Sobczyńska-Tomaszewska, Mariusz Ołtarzewski, Kamila Czerska, et al.American Journal of Medical Genetics. Part A|March 9, 2006
The ARX mutations: a frequent cause of X-linked mental retardationMagdalena Nawara, Krzysztof Szczaluba, Karine Poirier, et al.Pageof 9