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Diabetes/Metabolism Research and Reviews
|
March 23, 2005
Gly482Ser polymorphism of the peroxisome proliferator-activated receptor-gamma coactivator-1 gene might be a risk factor for diabetic retinopathy in Slovene population (Caucasians) with type 2 diabetes and the Pro12Ala polymorphism of the PPARgamma gene is not
Mojca Globocnik Petrovic, Tanja Kunej, Borut Peterlin, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2023
Perception of genomic newborn screening among peripartum mothers
Bernarda Prosenc, Mojca Cizek Sajko, Gorazd Kavsek, et al.
Journal of Human Genetics
|
December 6, 2006
Patients with primary cataract as a genetic pool of DMPK protomutation
Igor Medica, Natasa Teran, Marija Volk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 22, 2009
Gene expression changes in blood as a putative biomarker for Huntington's disease
Luca Lovrecic, Andrej Kastrin, Jan Kobal, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Genital anomalies in a patient with Treacher Collins syndrome
Karin Writzl, Jera Jeruc, Michael Oldridge, et al.
Journal of Assisted Reproduction and Genetics
|
December 18, 2016
Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion
Anita Barišić, Nina Pereza, Alenka Hodžić, et al.
Pflugers Archiv : European Journal of Physiology
|
February 9, 2017
Angiotensin-converting enzyme gene polymorphism as a cardiovascular risk factor in children
Nataša Marčun Varda, Borut Peterlin, Stanislava Umek Bradač, et al.
Medical and Pediatric Oncology
|
February 12, 2002
Single signal of the Williams syndrome chromosome region 1 gene in hyperploidic bone marrow cells of acute lymphoblastic leukemia in a Williams syndrome patient
Vida Culic, Srdjana Culic, Visnja Armanda, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
December 1, 2007
Association of angiotensin-converting enzyme/DD genotype with sarcoidosis susceptibility in Slovenian patients
Barbara Salobir, Igor Medica, Marjeta Tercelj, et al.
Acta Neurologica Belgica
|
February 5, 2022
A case report of a novel GNB1 pathogenic variant and the response to deep brain stimulation
Gloria Rožmarić, Mario Hero, Valentino Rački, et al.
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of 28
Search research articles
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Showing results (101-110 of 274) with videos related to
Sort By:
Page
of 28
Diabetes/Metabolism Research and Reviews
|
March 23, 2005
Gly482Ser polymorphism of the peroxisome proliferator-activated receptor-gamma coactivator-1 gene might be a risk factor for diabetic retinopathy in Slovene population (Caucasians) with type 2 diabetes and the Pro12Ala polymorphism of the PPARgamma gene is not
Mojca Globocnik Petrovic, Tanja Kunej, Borut Peterlin, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2023
Perception of genomic newborn screening among peripartum mothers
Bernarda Prosenc, Mojca Cizek Sajko, Gorazd Kavsek, et al.
Journal of Human Genetics
|
December 6, 2006
Patients with primary cataract as a genetic pool of DMPK protomutation
Igor Medica, Natasa Teran, Marija Volk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 22, 2009
Gene expression changes in blood as a putative biomarker for Huntington's disease
Luca Lovrecic, Andrej Kastrin, Jan Kobal, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Genital anomalies in a patient with Treacher Collins syndrome
Karin Writzl, Jera Jeruc, Michael Oldridge, et al.
Journal of Assisted Reproduction and Genetics
|
December 18, 2016
Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion
Anita Barišić, Nina Pereza, Alenka Hodžić, et al.
Pflugers Archiv : European Journal of Physiology
|
February 9, 2017
Angiotensin-converting enzyme gene polymorphism as a cardiovascular risk factor in children
Nataša Marčun Varda, Borut Peterlin, Stanislava Umek Bradač, et al.
Medical and Pediatric Oncology
|
February 12, 2002
Single signal of the Williams syndrome chromosome region 1 gene in hyperploidic bone marrow cells of acute lymphoblastic leukemia in a Williams syndrome patient
Vida Culic, Srdjana Culic, Visnja Armanda, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
December 1, 2007
Association of angiotensin-converting enzyme/DD genotype with sarcoidosis susceptibility in Slovenian patients
Barbara Salobir, Igor Medica, Marjeta Tercelj, et al.
Acta Neurologica Belgica
|
February 5, 2022
A case report of a novel GNB1 pathogenic variant and the response to deep brain stimulation
Gloria Rožmarić, Mario Hero, Valentino Rački, et al.
Page
of 28