City as an Object of Ecological and Economic Researches: the Example of Russian Cities by N. V. Shcherbakova, M. M. Khaikin

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SEMANTICS OF NOMINAL PERSONIFICATIONS IN POPULAR SCIENCE LINGUISTIC TEXTS by V. F. Kryukova, N. V. Shcherbakova

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EXOME SEQUENCING AND THE DIAGNOSTICS OF COMPLEX DISEASE PREDISPOSITION IN PREVENTIVE MEDICINE by N. V. Shcherbakova, A. N. Meshkov, S. A. Boytsov

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EVALUATION OF NATURAL POTENTIAL OF THE AREAS IN PETER THE GREAT BAY (JAPAN SEA) FOR COLLECTING OF OYSTER SPAT by S. A. Lyashenko, N. V. Shcherbakova, O. B. Gostyuhina

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Indications for genetic examinations in children with bradyarrhythmias by E. B. Polyakova, N. V. Shcherbakova, M. A. Shkolnikova

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Hypertrophic cardiomyopathy caused by mutations in the <I>PRKAG2</I> gene by I. V. Leontyeva, N. V. Shcherbakova, E. P. Kalachanova, S. A. Thermosesov, V. S. Sukhorukov

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Phenotypic variability and modifier variants in children with hereditary heart diseases by N. V. Shcherbakova, A. B. Zhironkina, V. Yu. Voinova, R. A. Ildarova, M. A. Shkolnikova

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A rare combination of monogenic connective tissue diseases — Marfan and Stickler syndromes — in one patient by E. A. Nikolaeva, A. N. Semyachkina, G. V. Dzhivanshiryan, N. V. Shcherbakova, A. V. Smirnova

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PHARMACOGENETIC TESTING OPPORTUNITIES IN CARDIOLOGY BASED ON EXOME SEQUENCING by N. V. Shcherbakova, A. I. Ershova, A. A. Suvorova, E. Y. Hlebus, A. N. Meshkov, S. A. Boytsov

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Acute myocardial infarction in the postpartum period in the young woman with protein C deficiency by E. S. Eniseeva, K. V. Protasov, Y. A. Reut, O. M. Senderova, N. V. Shcherbakova, N. V. Petronchak

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PHARMACOGENETIC TESTING OPPORTUNITIES IN CARDIOLOGY BASED ON EXOME SEQUENCING by N. V. Shcherbakova, A. I. Ershova, A. A. Suvorova, E. Y. Hlebus, A. N. Meshkov, S. A. Boytsov

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Phenotypical features of heterozygous familial hypercholesterolemia in individuals with LDLR or APOB gene mutations by A. N. Meshkov, A. I. Ershova, N. V. Shcherbakova, T. A. Rozhkova, M. V. Kalinina, V. V. Kukharchuk, S. A. Boytsov

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DIFFERENTIAL DIAGNOSIS OF HEREDITARY SYNDROME OF HYPOCHOLESTEROLEMIA BY USING EXOMIC SEQUENCING by A. I. Yershova, N. V. Shcherbakova, A. A. Suvorova, E. Y. Hlebus, I. V. Sidonets, A. N. Meshkov, S. A. Boytsov

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DIFFERENTIAL DIAGNOSIS OF HEREDITARY SYNDROME OF HYPOCHOLESTEROLEMIA BY USING EXOMIC SEQUENCING by A. I. Yershova, N. V. Shcherbakova, A. A. Suvorova, E. Y. Hlebus, I. V. Sidonets, A. N. Meshkov, S. A. Boytsov

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LIPID PROFILE AND GENETIC MARKERS ASSOCIATED WITH THE LEVEL OF OXIDIzED LOW DENSITY LIPOPROTEIDES by E. Yu. Khlebus, А. N. Meshkov, V. Z. Lankin, А. A. Orlovsky, А. V. Kiseleva, N. V. Shcherbakova, А. А. Zharikova, А. I. Ershova, А. К. Tikhaze, Е. B. Yarovaya, I. Е. Chazova, S. А. Boytsov

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DES GENE MUTATION IN A FAMILY OF PROBAND WITH MYOFIBRILLARY MYOPATHY AND NON-COMPACTION CARDIOMYOPATHY, RESULTED IN CARDIAC TRANSPLANTATION by R. P. Myasnikov, N. V. Shcherbakova, О. V. Kulikova, А. N. Meshkov, M. S. Kharlap, А. V. Kiseleva, А. А. Zharikova, Е. L. Dadali, N. A. Semenova, S. N. Koretsky, О. V. Blagova, Е. А. Mershina, V. Е. Sinitsyn, О. М. Drapkina, S. А. Boytsov

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