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Journal of Applied Genetics|August 20, 2010

Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patientsK Czerska, A Sobczynska-Tomaszewska, D Sands, et al.

Clinical Genetics|May 29, 2016

Hypomyelinating leukodystrophies - a molecular insight into the white matter pathologyA Charzewska, J Wierzba, E Iżycka-Świeszewska, et al.

Neurologia I Neurochirurgia Polska|August 30, 2013

Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patientsD Koziorowski, D Hoffman-Zacharska, J Sławek, et al.

Medycyna Wieku Rozwojowego|October 3, 2000

[Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland]I Aznarez, J Bal, T Casals, et al.

Fish & Shellfish Immunology|September 15, 2005

Passive transfer of maternal antibodies and their existence in eggs, larvae and fry of Indian major carp, Labeo rohita (Ham.)P Swain, S Dash, J Bal, et al.

Journal of Applied Genetics|January 27, 2020

Novel and recurrent variants of ATP2C1 identified in patients with Hailey-Hailey diseaseJ Sawicka, A Kutkowska-Kaźmierczak, K Woźniak, et al.

Immunogenetics|May 10, 2000

Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group BW Wiszniewski, M C Fondaneche, N Lambert, et al.

Journal of Applied Genetics|October 4, 2015

Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlationK Wertheim-Tysarowska, M Ołdak, A Giza, et al.

Clinical Genetics|July 15, 2018

The power of the Mediator complex-Expanding the genetic architecture and phenotypic spectrum of MED12-related disordersA Charzewska, R Maiwald, K Kahrizi, et al.

Human Genetics|May 8, 2000

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East EuropeT Dörk, M Macek, F Mekus, et al.

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Showing results (41-50 of 50) with videos related to

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You have reached the last page of results.This site can display upto 50 results.

Journal of Applied Genetics|August 20, 2010

Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patientsK Czerska, A Sobczynska-Tomaszewska, D Sands, et al.

Clinical Genetics|May 29, 2016

Hypomyelinating leukodystrophies - a molecular insight into the white matter pathologyA Charzewska, J Wierzba, E Iżycka-Świeszewska, et al.

Neurologia I Neurochirurgia Polska|August 30, 2013

Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patientsD Koziorowski, D Hoffman-Zacharska, J Sławek, et al.

Medycyna Wieku Rozwojowego|October 3, 2000

[Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland]I Aznarez, J Bal, T Casals, et al.

Fish & Shellfish Immunology|September 15, 2005

Passive transfer of maternal antibodies and their existence in eggs, larvae and fry of Indian major carp, Labeo rohita (Ham.)P Swain, S Dash, J Bal, et al.

Journal of Applied Genetics|January 27, 2020

Novel and recurrent variants of ATP2C1 identified in patients with Hailey-Hailey diseaseJ Sawicka, A Kutkowska-Kaźmierczak, K Woźniak, et al.

Immunogenetics|May 10, 2000

Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group BW Wiszniewski, M C Fondaneche, N Lambert, et al.

Journal of Applied Genetics|October 4, 2015

Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlationK Wertheim-Tysarowska, M Ołdak, A Giza, et al.

Clinical Genetics|July 15, 2018

The power of the Mediator complex-Expanding the genetic architecture and phenotypic spectrum of MED12-related disordersA Charzewska, R Maiwald, K Kahrizi, et al.

Human Genetics|May 8, 2000

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East EuropeT Dörk, M Macek, F Mekus, et al.

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