<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">agx</journal-id><journal-title-group><journal-title xml:lang="ru">Андрология и генитальная хирургия</journal-title><trans-title-group xml:lang="en"><trans-title>Andrology and Genital Surgery</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2070-9781</issn><issn pub-type="epub">2412-8902</issn><publisher><publisher-name></publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17650/2070-9781-2022-23-4-81-89</article-id><article-id custom-type="elpub" pub-id-type="custom">agx-619</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>ОРИГИНАЛЬНАЯ СТАТЬЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL REPORT</subject></subj-group></article-categories><title-group><article-title>Параметры спермограммы у мужчин – носителей робертсоновских транслокаций (13;14)</article-title><trans-title-group xml:lang="en"><trans-title>Semen parameters in male carriers of Robertsonian translocations (13;14)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5048-5486</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Андреева</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Andreeva</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522 Москва, ул. Москворечье, 1</p></bio><bio xml:lang="en"><p>1 Moskvorech’e St., Moscow 115522</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3603-4838</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Курило</surname><given-names>Л. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Kurilo</surname><given-names>L. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522 Москва, ул. Москворечье, 1</p></bio><bio xml:lang="en"><p>1 Moskvorech’e St., Moscow 115522</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0580-5575</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Штаут</surname><given-names>М. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Shtaut</surname><given-names>M. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522 Москва, ул. Москворечье, 1</p></bio><bio xml:lang="en"><p>1 Moskvorech’e St., Moscow 115522</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7032-0793</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Седова</surname><given-names>А. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Sedova</surname><given-names>A. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522 Москва, ул. Москворечье, 1</p></bio><bio xml:lang="en"><p>1 Moskvorech’e St., Moscow 115522</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4618-2466</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сорокина</surname><given-names>Т. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Sorokina</surname><given-names>T. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522 Москва, ул. Москворечье, 1</p></bio><bio xml:lang="en"><p>1 Moskvorech’e St., Moscow 115522</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7615-8512</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Черных</surname><given-names>В. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Chernykh</surname><given-names>V. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Вячеслав Борисович Черных</p><p>115522 Москва, ул. Москворечье, 1</p></bio><bio xml:lang="en"><p>Vyacheslav Borisovich Chernykh </p><p>1 Moskvorech’e St., Moscow 115522</p></bio><email xlink:type="simple">chernykh@med-gen.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Медико-генетический научный центр им. акад. Н.П. Бочкова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>N.P. Bochkov Research Centre for Medical Genetics</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>09</day><month>01</month><year>2023</year></pub-date><volume>23</volume><issue>4</issue><fpage>81</fpage><lpage>89</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Андреева М.В., Курило Л.Ф., Штаут М.И., Седова А.О., Сорокина Т.М., Черных В.Б., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Андреева М.В., Курило Л.Ф., Штаут М.И., Седова А.О., Сорокина Т.М., Черных В.Б.</copyright-holder><copyright-holder xml:lang="en">Andreeva M.V., Kurilo L.F., Shtaut M.I., Sedova A.O., Sorokina T.M., Chernykh V.B.</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://agx.elpub.ru/jour/article/view/619">https://agx.elpub.ru/jour/article/view/619</self-uri><abstract><sec><title>Введение</title><p>Введение. Робертсоновские транслокации (РТ) являются наиболее распространенным типом сбалансированных хромосомных аномалий. Мужчины – носители РТ имеют повышенный риск нарушений репродукции, однако причины этого недостаточно изучены.</p><p>Цель исследования – оценить параметры спермограммы у мужчин – носителей РТ (13;14).</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Обследованы 24 мужчины с кариотипом 45,XY,der(13;14)(q10;q10), обратившихся в связи с бесплодием в браке (n = 23) или привычным невынашиванием беременности у супруги (n = 1). Результаты. У 18 (75 %) пациентов выявлена олигоастенотератозооспермия, у 3 (13 %) пациентов – астенотератозооспермия, у 2 (8 %) – азооспермия. Нормозооспермия диагностирована только у 1 (4 %) пациента, у него в анамнезе – привычное невынашивание беременности у супруги.</p></sec><sec><title>Выводы</title><p>Выводы. Бесплодие у обследованных мужчин – носителей РТ связано с нарушением сперматогенеза, у большинства пациентов приводящим к олигоастенотератозооспермии.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Background</title><p>Background. Robertsonian translocations (RTs) are the most common type of balanced chromosomal abnormalities. RT male carriers have an increased risk of reproductive disorders, but the causes of this still are not clear enough.</p></sec><sec><title>Aim</title><p>Aim. To evaluate semen parameters in RT(13;14) male carriers.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. 24 men with 45,XY,der(13;14)(q10;q10) karyotype and infertility (n = 23) or recurrent pregnancy loss in spouse (n = 1).</p></sec><sec><title>Results</title><p>Results. Oligoasthenoteratozoospermia was detected in 18 (75 %) patients, asthenoteratozoospermia in 3 (13 %) patients, and azoospermia in 2 (8 %) patients. Normozoospermia was detected in 1 (4 %) patient, whose wife had a history of recurrent pregnancy loss.</p></sec><sec><title>Conclusion</title><p>Conclusion. Infertility in the examined RT male carriers is associated with spermatogenesis disorders, in most cases resulted in oligozooasthenoteratozoospermia.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>робертсоновские транслокации</kwd><kwd>мужское бесплодие</kwd><kwd>кариотип</kwd><kwd>эякулят</kwd><kwd>спермограмма</kwd><kwd>олигозооспермия</kwd><kwd>азооспермия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Robertsonian translocations</kwd><kwd>male infertility</kwd><kwd>karyotype</kwd><kwd>sperm</kwd><kwd>semen analysis</kwd><kwd>oligozoospermia</kwd><kwd>azoospermia</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках проекта «Многоцентровая исследовательская биоресурсная коллекция “Репродуктивное здоровье человека”» № 15.БРК.21.0008 Министерства науки и высшего образования Российской Федерации.</funding-statement><funding-statement xml:lang="en">The work was carried out within the framework of the project “Multicenter research bioresource collection “Human Reproductive Health” No. 15.BRK.21.0008 of the Ministry of Science and Higher Education of the Russian Federation.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Nielsen J., Wohlert M. Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Hum Genet 1991;87(1):81–3. DOI: 10.1007/BF01213097</mixed-citation><mixed-citation xml:lang="en">Nielsen J., Wohlert M. Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Hum Genet 1991;87(1):81–3. DOI: 10.1007/BF01213097</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">McKinlay Gardner R.J. et al. Robertsonian translocations. In: Gardner and sutherland’s chromosome abnormalities and genetic counseling. Ed. by R.J. McKinlay Gardner, D.J. Armour. 5th edn. Oxford monographs on medical genetics. New York: Oxford Academic, 2018. (online edn.). DOI: 10.1093/med/9780199329007.003.0007</mixed-citation><mixed-citation xml:lang="en">McKinlay Gardner R.J. et al. Robertsonian translocations. In: Gardner and sutherland’s chromosome abnormalities and genetic counseling. Ed. by R.J. McKinlay Gardner, D.J. Armour. 5th edn. Oxford monographs on medical genetics. New York: Oxford Academic, 2018. (online edn.). DOI: 10.1093/med/9780199329007.003.0007</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">De Braekeleer M., Dao T.N. Cytogenetic studies in male infertility: a review. Hum Reprod 1991;6(2):245–50. PMID: 2056021.</mixed-citation><mixed-citation xml:lang="en">De Braekeleer M., Dao T.N. Cytogenetic studies in male infertility: a review. Hum Reprod 1991;6(2):245–50. PMID: 2056021.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Van Assche E., Bonduelle M., Tournaye H. et al. Cytogenetics of infertile men. Hum Reprod 1996;11(Suppl 4):1–24. DOI: 10.1093/humrep/11.suppl_4.1</mixed-citation><mixed-citation xml:lang="en">Van Assche E., Bonduelle M., Tournaye H. et al. Cytogenetics of infertile men. Hum Reprod 1996;11(Suppl 4):1–24. DOI: 10.1093/humrep/11.suppl_4.1</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Ogur G., Van Assche E., Vegetti W. et al. Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers. Mol Hum Reprod 2006;12(3):209–15. DOI: 10.1093/molehr/gah253</mixed-citation><mixed-citation xml:lang="en">Ogur G., Van Assche E., Vegetti W. et al. Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers. Mol Hum Reprod 2006;12(3):209–15. DOI: 10.1093/molehr/gah253</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Luciani J.M., Guichaoua M.R., Mattei A., Morazzani M.R. Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle. Cytogenet Cell Genet 1984;38(1):14–22. DOI: 10.1159/000132023</mixed-citation><mixed-citation xml:lang="en">Luciani J.M., Guichaoua M.R., Mattei A., Morazzani M.R. Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle. Cytogenet Cell Genet 1984;38(1):14–22. DOI: 10.1159/000132023</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Rosenmann A., Wahrman J., Richler C. et al. Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterility. Cytogenet Cell Genet 1985;39(1):19–29. DOI: 10.1159/000132098</mixed-citation><mixed-citation xml:lang="en">Rosenmann A., Wahrman J., Richler C. et al. Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterility. Cytogenet Cell Genet 1985;39(1):19–29. DOI: 10.1159/000132098</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Godo A., Blanco J., Vidal F. et al. Altered segregation pattern and numerical chromosome abnormalities interrelate in spermatozoa from Robertsonian translocation carriers. Reprod Biomed Online 2015;31(1):79–88. DOI: 10.1016/j.rbmo.2015.04.003</mixed-citation><mixed-citation xml:lang="en">Godo A., Blanco J., Vidal F. et al. Altered segregation pattern and numerical chromosome abnormalities interrelate in spermatozoa from Robertsonian translocation carriers. Reprod Biomed Online 2015;31(1):79–88. DOI: 10.1016/j.rbmo.2015.04.003</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Kovaleva N.V. Examination of rates and spectrums of robertsonian translocations in the general population and in patients with reproductive disorders. Russ J Genet 2018;54(4):489–93. DOI: 10.1134/S1022795418040099</mixed-citation><mixed-citation xml:lang="en">Kovaleva N.V. Examination of rates and spectrums of robertsonian translocations in the general population and in patients with reproductive disorders. Russ J Genet 2018;54(4):489–93. DOI: 10.1134/S1022795418040099</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. 4th edn. Cambridge: Cambridge University Press, 1999.</mixed-citation><mixed-citation xml:lang="en">WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. 4th edn. Cambridge: Cambridge University Press, 1999.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">WHO laboratory manual for the examination and processing of human semen. 5th edn. Geneva, Swtizerland: WHO, 2010.</mixed-citation><mixed-citation xml:lang="en">WHO laboratory manual for the examination and processing of human semen. 5th edn. Geneva, Swtizerland: WHO, 2010.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Antonelli A., Gandini L., Petrinelli P. et al. Chromosomal alterations and male infertility. J Endocrinol Invest 2000;23(10):677–83. DOI: 10.1007/BF03343793</mixed-citation><mixed-citation xml:lang="en">Antonelli A., Gandini L., Petrinelli P. et al. Chromosomal alterations and male infertility. J Endocrinol Invest 2000;23(10):677–83. DOI: 10.1007/BF03343793</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Ferfouri F., Selva J., Boitrelle F. et al. The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type. Fertil Steril 2011;96(6):1337–43. DOI: 10.1016/j.fertnstert.2011.09.008</mixed-citation><mixed-citation xml:lang="en">Ferfouri F., Selva J., Boitrelle F. et al. The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type. Fertil Steril 2011;96(6):1337–43. DOI: 10.1016/j.fertnstert.2011.09.008</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Vozdova M., Oracova E., Kasikova K. et al. Balanced chromosomal translocations in men: relationships among semen parameters, chromatin integrity, sperm meiotic segregation and aneuploidy. J Assist Reprod Genet 2013;30(3):391–405. DOI: 10.1007/s10815-012-9921-9</mixed-citation><mixed-citation xml:lang="en">Vozdova M., Oracova E., Kasikova K. et al. Balanced chromosomal translocations in men: relationships among semen parameters, chromatin integrity, sperm meiotic segregation and aneuploidy. J Assist Reprod Genet 2013;30(3):391–405. DOI: 10.1007/s10815-012-9921-9</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Pastuszek E., Kiewisz J., Kulwikowska P.M. et al. Sperm parameters and DNA fragmentation of balanced chromosomal rearrangements carriers. Folia Histochem Cytobiol 2015;53(4):314–21. DOI: 10.5603/fhc.a2015.0032</mixed-citation><mixed-citation xml:lang="en">Pastuszek E., Kiewisz J., Kulwikowska P.M. et al. Sperm parameters and DNA fragmentation of balanced chromosomal rearrangements carriers. Folia Histochem Cytobiol 2015;53(4):314–21. DOI: 10.5603/fhc.a2015.0032</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Lamotte A., Martinez G., Devillard F. et al. Is sperm FISH analysis still useful for Robertsonian translocations? Meiotic analysis for 23 patients and review of the literature. Basic Clin Androl 2018;28:5. DOI: 10.1186/s12610-018-0069-z</mixed-citation><mixed-citation xml:lang="en">Lamotte A., Martinez G., Devillard F. et al. Is sperm FISH analysis still useful for Robertsonian translocations? Meiotic analysis for 23 patients and review of the literature. Basic Clin Androl 2018;28:5. DOI: 10.1186/s12610-018-0069-z</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Mayeur A., Ahdad N., Hesters L. et al. Chromosomal translocations and semen quality: a study on 144 male translocation carriers. Reprod Biomed Online 2019;38(1):46–55. DOI: 10.1016/j.rbmo.2018.10.003</mixed-citation><mixed-citation xml:lang="en">Mayeur A., Ahdad N., Hesters L. et al. Chromosomal translocations and semen quality: a study on 144 male translocation carriers. Reprod Biomed Online 2019;38(1):46–55. DOI: 10.1016/j.rbmo.2018.10.003</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Gatimel N., Moreau J., Parinaud J., Léandri R.D. Sperm morphology: assessment, pathophysiology, clinical relevance, and state of the art in 2017. Andrology 2017;5(5):845–62. DOI: 10.1111/andr.12389</mixed-citation><mixed-citation xml:lang="en">Gatimel N., Moreau J., Parinaud J., Léandri R.D. Sperm morphology: assessment, pathophysiology, clinical relevance, and state of the art in 2017. Andrology 2017;5(5):845–62. DOI: 10.1111/andr.12389</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Олефир Ю.В., Монаков Д.М. Клиническое значение морфологии сперматозоидов в выборе метода лечения мужского бесплодия. Экспериментальная и клиническая урология 2021;14(3):127–32. DOI: 10.29188/2222-8543-2021-14-3-127-132</mixed-citation><mixed-citation xml:lang="en">Olefir Yu.V., Monakov D.M. Clinical significance of sperm morphology in male infertility treatment. Eksperimentalnaya i klinicheskaya urologiya = Experimental and Clinical Urology 2021;14(3):127–32. (In Russ.). DOI: 10.29188/2222-8543-2021-14-3-127-132</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Гамидов С.И., Овчинников Р.И., Попова А.Ю. и др. Эффективность программ вспомогательных репродуктивных технологий в зависимости от характера изменений спермограммы. Андрология и генитальная хирургия 2018;19(2):82–7. DOI: 10.17650/2070-9781-2018-19-2-82-87</mixed-citation><mixed-citation xml:lang="en">Gamidov S.I., Ovchinnikov R.I., Popova A.Yu. et al. Effectiveness of assisted reproductive treatment programs depending on the characteristics of spermogram change. Andrologiya i genital’naya khirurgiya = Andrology and Genital Surgery 2018;19(2):82–7. (In Russ.). DOI: 10.17650/2070-9781-2018-19-2-82-87</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Гамидов С.И., Овчинников Р.И., Попова А.Ю. и др. Роль мужского фактора бесплодия в программе вспомогательных репродуктивных технологий (обзор литературы). Андрология и генитальная хирургия 2017;18(3):28–36. DOI: 10.17650/2070- 9781-2017-18-3-28-36</mixed-citation><mixed-citation xml:lang="en">Gamidov S.I., Ovchinnikov R.I., Popova A.Yu. et al. Role of male infertility in assisted reproductive technology programs (a literature review). Andrologiya i genital’naya khirurgiya = Andrology and Genital Surgery 2017;18(3):28–36. (In Russ.). DOI: 10.17650/2070-9781-2017-18-3-28-36</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu S., Zhu Y., Zhang F. et al. FISH analysis of numerical chromosomal abnormalities in the sperm of robertsonian translocation der(13; 14)(q10;q10) carriers. Front Genet 2022;13:1010568. DOI: 10.3389/fgene.2022.1010568</mixed-citation><mixed-citation xml:lang="en">Zhu S., Zhu Y., Zhang F. et al. FISH analysis of numerical chromosomal abnormalities in the sperm of robertsonian translocation der(13; 14)(q10;q10) carriers. Front Genet 2022;13:1010568. DOI: 10.3389/fgene.2022.1010568</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Johannisson R., Schwinger E., Wolff H.H. et al. The effect of 13;14 Robertsonian translocations on germ-cell differentiation in infertile males. Cytogenet Cell Genet 1993;63(3):151–5. DOI: 10.1159/000133524</mixed-citation><mixed-citation xml:lang="en">Johannisson R., Schwinger E., Wolff H.H. et al. The effect of 13;14 Robertsonian translocations on germ-cell differentiation in infertile males. Cytogenet Cell Genet 1993;63(3):151–5. DOI: 10.1159/000133524</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Page S.L., Shin J.C., Han J.Y. et al. Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation. Hum Mol Genet 1996;5(9):1279–88. DOI: 10.1093/hmg/5.9.1279</mixed-citation><mixed-citation xml:lang="en">Page S.L., Shin J.C., Han J.Y. et al. Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation. Hum Mol Genet 1996;5(9):1279–88. DOI: 10.1093/hmg/5.9.1279</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Morel F., Douet-Guilbert N., Le Bris M.J., Amice V. et al. Chromosomal abnormalities in couples undergoing intracytoplasmic sperm injection. A study of 370 couples and review of the literature. Int J Androl 2004;27(3):178–82. DOI: 10.1111/j.1365-2605.2004.00472.x</mixed-citation><mixed-citation xml:lang="en">Morel F., Douet-Guilbert N., Le Bris M.J., Amice V. et al. Chromosomal abnormalities in couples undergoing intracytoplasmic sperm injection. A study of 370 couples and review of the literature. Int J Androl 2004;27(3):178–82. DOI: 10.1111/j.1365-2605.2004.00472.x</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
