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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.25557/2073-7998.2020.11.54-57</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-1796</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BRIEF REPORT</subject></subj-group></article-categories><title-group><article-title>Частота микроделеций Y-хромосомы у армянских мужчин с бесплодием</article-title><trans-title-group xml:lang="en"><trans-title>Frequency of Y chromosome microdeletions in Armenian infertile men</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шахсуварян</surname><given-names>Г. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Shahsuvaryan</surname><given-names>G. .</given-names></name></name-alternatives><email xlink:type="simple">gshahsuvaryan@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Караханян</surname><given-names>Р. .</given-names></name><name name-style="western" xml:lang="en"><surname>Karakhanyan</surname><given-names>R. .</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Саркисян</surname><given-names>Т. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Sarkisian</surname><given-names>T. .</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ижевская</surname><given-names>В. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Izhevskaya</surname><given-names>V. .</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Центр медицинской гeнетики и первичной охраны здоровья</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Center of Medical Genetics and Primary Health Care</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «Медико-генетический научный центр имени академика Н.П. Бочкова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Centre for Medical Genetics</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>02</day><month>02</month><year>2021</year></pub-date><volume>19</volume><issue>11</issue><fpage>54</fpage><lpage>57</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шахсуварян Г.Р., Караханян Р..., Саркисян Т.Ф., Ижевская В.Л., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Шахсуварян Г.Р., Караханян Р..., Саркисян Т.Ф., Ижевская В.Л.</copyright-holder><copyright-holder xml:lang="en">Shahsuvaryan G..., Karakhanyan R..., Sarkisian T..., Izhevskaya V...</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.medgen-journal.ru/jour/article/view/1796">https://www.medgen-journal.ru/jour/article/view/1796</self-uri><abstract><p>Микроделеции длинного плеча Y-хромосомы являются частой генетической причиной мужского бесплодия, связанного с азооспермией и олигозооспермией. В различных этнических группах частота встречаемости микроделеций Y-хромосомы может существенно варьировать, а их спектр иметь определенные особенности. Целью представленного исследования являлось определение частоты и структуры микроделеционных изменений локуса AZF у мужчин армянской национальности с бесплодием для оптимизации диагностических и лечебных мероприятий с применением вспомогательных репродуктивных технологий.</p></abstract><trans-abstract xml:lang="en"><p>The long arm of the Y chromosome microdeletions are common genetic cause of male infertility, related with azoospermia and oligozoospermia. The frequency of various Y-chromosome microdeletions can vary significantly in different ethnic groups and have certain features. The aim of the presented research is to determine the frequency and spectrum of AZF (azoospermia factor) microdeletions in infertile men of Armenian nationality, in order to optimize diagnostic and therapeutic measures using assisted reproductive technologies.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>микроделеции</kwd><kwd>Y-хромосома</kwd><kwd>мужское бесплодие</kwd><kwd>сперматогенез</kwd></kwd-group><kwd-group xml:lang="en"><kwd>microdeletions</kwd><kwd>Y-chromosome</kwd><kwd>male infertility</kwd><kwd>spermatogenesis</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Kleiman S.E., Bar-Shira MaymonB., YogevL., PazG., YavetzH., The prognostic role of the extent of Y microdeletion on spermatogenesis and maturity of Sertoli cells. Hum. 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