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| Issue | Title | |
| Vol 10, No 6 (2014) | PHARMACOGENETIC TESTING OPPORTUNITIES IN CARDIOLOGY BASED ON EXOME SEQUENCING | Abstract similar documents |
| N. V. Shcherbakova, A. I. Ershova, A. A. Suvorova, E. Y. Hlebus, A. N. Meshkov, S. A. Boytsov | ||
| "... экзомного секвенирования у пациента с кардиологической патологией. Материал и методы. Проведено ..." | ||
| Vol 15, No 4 (2019) | Pathogenic Variant Rs1471414348of the TTN Gene in the Patient with Familial Left Venticular Noncompaction Cardiomyopathy | Abstract similar documents |
| O. V. Kulikova, A. N. Meshkov, R. P. Myasnikov, A. V. Kiseleva, S. N. Koretsky, A. A. Zharikova, M. S. Kharlap, E. A. Mershina, V. E. Sinitsyn, O. P. Skirko, I. A. Efimova, M. S. Pokrovskaya, S. A. Boytsov, O. M. Drapkina | ||
| "... желудочка, отсутствие нарушений ритма и дилатации сердца у матери пробанда. При экзомном секвенировании ..." | ||
| Vol 16, No 3 (2020) | New Variant of MYH7 Gene Nucleotide Sequence in Familial Non-Compaction Cardiomyopathy with Benign Course | Abstract PDF (Eng) similar documents |
| R. P. Myasnikov, O. V. Kulikova, A. N. Meshkov, A. V. Kiseleva, A. O. Shumarina, S. N. Koretskiy, A. A. Zharikova, M. G. Divashuk, M. S. Kharlap, S. E. Serduk, E. A. Mershina, V. E. Sinitsyn, S. A. Boytsov, O. M. Drapkina | ||
| "... родственникам 1 и 2 степени родства было проведено клинико-инструментальное обследование и экзомное ..." | ||
| Vol 10, No 5 (2014) | DIFFERENTIAL DIAGNOSIS OF HEREDITARY SYNDROME OF HYPOCHOLESTEROLEMIA BY USING EXOMIC SEQUENCING | Abstract similar documents |
| A. I. Yershova, N. V. Shcherbakova, A. A. Suvorova, E. Y. Hlebus, I. V. Sidonets, A. N. Meshkov, S. A. Boytsov | ||
| "... гипохолестеринемии с применением метода экзомного секвенирования, позволяющего секвенировать большинство областей ..." | ||
| Vol 22, No 1 (2026) | Atrial fibrillation with progressive left ventricular dysfunction: what lies beneath the tip of the iceberg (clinical case)? | Abstract similar documents |
| O. V. Blagova, D. Kh. Ainetdinova, D. S. Panin, D. A. Tsaregorodtsev, V. P. Sedov, E. A. Kogan | ||
| "... устьев легочных вен, сохраняются пароксизмы ФП. При полноэкзомном секвенировании выявлен вариант в гене ..." | ||
| Vol 21, No 6 (2025) | Conduction disorders as an early marker of cardiac glycogenosis (PRKAG2 syndrome) | Abstract similar documents |
| O. V. Kulikova, R. P. Myasnikov, A. V. Kiseleva, E. V. Gagarina, D. A. Nefedova, A. A. Bukaeva, A. A. Zharikova, E. A. Mershina, A. N. Meshkov, O. M. Drapkina | ||
| "... -инструментальное обследование пробанда и его ближайших родственников, а также полноэкзомное секвенирование ..." | ||
| 1 - 6 of 6 Items | ||
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