Molecular genetic diagnosis of a heterozygous form of familial hypercholesterolemia at a young age: a clinical case von Olga V. Timoshchenko, Dinara E. Ivanoshchuk, Sergey E. Semaev, Lyudmila D. Latyntseva, Elena V. Shakhtshneider

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ASSOCIATION OF THE DELETION ALLELE OF THE INSERTION/DELETION POLYMORPHISM OF αIIbβ3 INTEGRIN GENE AND METABOLIC SYNDROME IN YOUNG NORTHERNERS von KORNEEVA, E. V., VOEVODA, M. I., SEMAEV, S. E., MAKSIMOV, V. N.

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