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Collegium Antropologicum|February 24, 2001
Characteristics of myotonic dystrophy in Istria: molecular genetic approach. Part II: Analysis of genetic polymorphismsI Medica, N Logar, B PeterlinMethods of Information in Medicine|January 22, 2010
Chi-square-based scoring function for categorization of MEDLINE citationsA Kastrin, B Peterlin, D HristovskiOptometry and Vision Science : Official Publication of the American Academy of Optometry|January 6, 1999
Bilateral macular dysplasia in fragile X syndromeB S Kranjc, A Brezigar, B PeterlinCollegium Antropologicum|January 15, 1999
Characteristics of myotonic dystrophy in Istria: molecular genetics approach--mutation analysisI Medica, N Logar, M Batagelj, et al.Pflugers Archiv : European Journal of Physiology|September 27, 2000
The Str mouse as a model for incontinentia pigmentiT Perkovic, D Duh, B Peterlin, et al.Clinical Genetics|July 6, 2005
Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart-hand syndrome?M Sinkovec, D Petrovic, M Volk, et al.Annales De Genetique|May 4, 2001
Joint effect of G1691A factor V point mutation and factor VII Arg/Gln(353) gene polymorphism on the risk of premature coronary artery diseaseD Petrovic, M Zorc, I Keber, et al.Studies in Health Technology and Informatics|February 24, 2001
A data mining approach to the development of a diagnostic test for male infertilityS Dzeroski, D Hristovski, T Kunej, et al.Angiology|May 2, 2001
Interaction between gene polymorphisms of renin-angiotensin system and metabolic risk factors in premature myocardial infarctionD Petrovic, M Zorc, V Kanic, et al.Folia Biologica|July 28, 2005
Are the T/C polymorphism of the CYP17 gene and the tetranucleotide repeat (TTTA) polymorphism of the CYP19 gene genetic markers for premature coronary artery disease in Caucasians?M Letonja, B Peterlin, D Bregar, et al.Pageof 8