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regulator gene (CFTR) mutations in the population, which is determined by genetic diversity and ethnicity

individuals of 5 Finno-Permic populations from the territories of the European part of the Russian Federation

ПОПУЛЯЦИОННО-ГЕНЕТИЧЕСКОЕ ИССЛЕДОВАНИЕ РАСПРЕДЕЛЕНИЯ И НАСЛЕДОВАНИЯ АЛЛЕЛЕЙ ГЕНА НЕЙРОПИЛИН-1 (NRP1) В БАШКОРТОСТАНЕPOPULATION GENETIC STUDY OF THE DISTRIBUTION AND INHERITANCE OF NEUROPILIN-1 (NRP1) GENE ALLELES

Background Genome-wide association studies have captured a large proportion of genetic variation

genetic predisposition

risk of developing disease outcomes from the general population. Clear cell renal cell carcinoma (cc

topography and its thinning, stretching, and protrusion. The hereditary or genetic theory of keratoconus

in the development of blood pressure elevation. The population of Tatars residing in the Volga-Ural region of Russia

sclerosis in populations of European ancestry, but the associations are not always reproducible in other

to the general population. The comorbidity between schizophrenia and depression suggests a potential coincidence

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