يعرض 1 - 10 نتائج من 97 نتيجة بحث عن '"Kudryavtseva, V"', وقت الاستعلام: 1.08s تنقيح النتائج
  1. 1
    دورية أكاديمية

    المساهمون: Bellussi, F, Roscioni, O, Rossi, E, Cardellini, A, Provenzano, M, Persichetti, L, Kudryavtseva, V, Sukhorukov, G, Asinari, P, Sebastiani, M, Fasano, M

    العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000852931100004; volume:48; firstpage:1; lastpage:10; numberofpages:10; journal:MRS BULLETIN; http://hdl.handle.net/2108/306050Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85137849506

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    دورية أكاديمية

    المساهمون: Bellussi, Fm, Roscioni, Om, Rossi, E, Cardellini, A, Provenzano, M, Persichetti, L, Kudryavtseva, V, Sukhorukov, G, Asinari, P, Sebastiani, M, Fasano, M

    مصطلحات موضوعية: Fluid, Interface, Nanoscale, Polymer, Wettability, Water

    وصف الملف: ELETTRONICO

    العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000852931100004; volume:48; firstpage:1; lastpage:10; numberofpages:10; journal:MRS BULLETIN; info:eu-repo/grantAgreement/EC/H2020/corda__h2020::45b16c683dbef78348b61e1658bb80c2; https://hdl.handle.net/11583/2972981Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85137849506; https://link.springer.com/article/10.1557/s43577-022-00380-9Test

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    دورية أكاديمية
  4. 4
    دورية أكاديمية

    المساهمون: Kudryavtseva, V., Boi, S., Read, J., Gould, D., Szewczyk, P. K., Stachewicz, U., Kiryukhin, M. V., Pastorino, L., Sukhorukov, G. B.

    وصف الملف: ELETTRONICO

    العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000633008700003; volume:202; firstpage:109527 - 1; lastpage:109527 - 10; numberofpages:10; journal:MATERIALS & DESIGN; https://hdl.handle.net/11567/1054181Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85100391107

  5. 5
    دورية أكاديمية

    المؤلفون: Kudryavtseva, V. A.1 valenkud@yandex.ru, Shigaeva, T. D.1 t.sh54@mail.ru

    المصدر: Russian Journal of General Chemistry. Dec2023, Vol. 93 Issue 13, p3391-3394. 4p.

    مصطلحات جغرافية: GULF of Finland

  6. 6
    دورية أكاديمية

    المصدر: Obstetrics, Gynecology and Reproduction; Vol 15, No 4 (2021); 379-389 ; Акушерство, Гинекология и Репродукция; Vol 15, No 4 (2021); 379-389 ; 2500-3194 ; 2313-7347

    وصف الملف: application/pdf

    العلاقة: https://www.gynecology.su/jour/article/view/1035/925Test; Quenby S., Gallos I.D., Dhillon-Smith R.K. et al. Miscarriage matters: the epidemiological, physical, psychological, and economic costs of early pregnancy loss. Lancet. 2021;397(10285):1658-67. https://doi.org/10.1016/S0140-6736Test(21)00682-6.; Miscarriage: worldwide reform of care is needed. Lancet. 2021;397(10285):1597. https://doi.org/10.1016/S0140-6736Test(21)00954-5.; Coomarasamy A., Gallos I.D., Papadopoulou A. et al. Sporadic miscarriage: evidence to provide effective care. Lancet. 2021;397(10285):1668-74. https://doi.org/10.1016/S0140-6736Test(21)00683-8.; Кудрявцева Е.В., Ковалёв В.В., Баранов И.И. и др. Роль хромосомных аберраций эмбриона в генезе привычного и спорадического невынашивания беременности. Вопросы гинекологии, акушерства и перинатологии. 2021;20(1):34-9. https://doi.org/10.20953/1726-1678-2021-1-34-39Test.; Кудрявцева Е.В., Ковалев В.В., Канивец И.В., Коростелев С.А. Современные возможности выявления хромосомных аномалий в абортивном материале. Уральский медицинский журнал. 2016;(11):5-8.; Kacprzak M., Chrzanowska M., Skoczylas B. et al. Genetic causes of recurrent miscarriages. Ginekol Pol. 2016;87(10):722-6. https://doi.org/10.5603/GP.2016.0075Test.; Sahoo T., Dzidic N., Strecker M.N. et al. Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges. Genet Med. 2017;19(1):83-9. https://doi.org/10.1038/gim.2016.69Test.; Coomarasamy A., Devall A.J., Brosens J.J. et al. Micronized vaginal progesterone to prevent miscarriage: a critical evaluation of randomized evidence. Am J Obstet Gynecol. 2020;223(2):167-76. https://doi.org/10.1016/j.ajog.2019.12.006Test.; ESHRE Guideline Group on RPL; Atik R.B., Christiansen O.B., Elson J. et al. ESHRE guideline: recurrent pregnancy loss. Hum Reprod Open. 2018;(2):hoy004. https://doi.org/10.1093/hropen/hoy004Test.; Адамян Л.В., Артымук Н.В., Белокриницкая Т.Е. и др. Выкидыш в ранние сроки беременности: диагностика и тактика ведения. Проблемы репродукции. 2018;24(S6):338-57.; Доброхотова Ю.Э., Мандрыкина Ж.А., Нариманова М.Р. Несостоявшийся выкидыш. Причины и возможности реабилитации. Российский вестник акушера-гинеколога. 2016;16(4):85-90. https://doi.org/10/17166/rosakush201616485-90Test.; Андреева М.Д., Капанадзе Д.Л., Самбурова Н.В. Акушерские и перинатальные исходы у пациенток с синдромом потери плода в анамнезе, генетическими и приобретенными формами тромбофилии. Акушерство, Гинекология и Репродукция. 2014;8(4):54-5.; Макацария А.Д., Хизроева Д.Х., Бицадзе В.О., Акиньшина С.В. Беременность и гомозиготные и сочетанные формы тромофилии у пациенток с тромботическим и акушерским отягощённым анамнезом. Тромбоз, гемостаз и реология. 2016;(S3):269-70.; Kamali M., Hantoushzadeh S., Borna S. et al. Association between thrombophilic genes polymorphisms and recurrent pregnancy loss susceptibility in the Iranian population: a systematic review and metaanalysis. Iran Biomed J. 2018;22(2):78-89. https://doi.org/10.22034/ibj.22.2.78Test.; Mehandjiev T.R., Tenno N.M., Nakura Y. et al. Impact of maternal methylenetetrahydrofolate reductase C677T polymorphism on intervillous and decidual pathology with pregnancy loss. J Obstet Gynaecol Res. 2019;45(1):78-85. https://doi.org/10.1111/jog.13798Test.; Ruixue W., Hongli Z., Zhihong Z. et al. The impact of semen quality, occupational exposure to environmental factors and lifestyle on recurrent pregnancy loss. J Assist Reprod Genet. 2013;30(11):1513-8. https://doi.org/10.1007/s10815-013-0091-1Test.; Anifandis G., Bounartzi T., Messini C.I. et al. The impact of cigarette smoking and alcohol consumption on sperm parameters and sperm DNA fragmentation (SDF) measured by Halosperm(®). Arch Gynecol Obstet. 2014;290(4):777-82. https://doi.org/10.1007/s00404-014-3281-xTest.; Pacey A.A. Environmental and lifestyle factors associated with sperm DNA damage. Hum Fertil (Camb). 2010;13(4):189-93. https://doi.org/10.3109/14647273.2010.531883Test.; Ковалев В.В., Кудрявцева Е.В. Молекулярно-генетические девиации и акушерская патология. Акушерство и гинекология. 2020;(1):28-31. https://doi.org/10.18565/aig.2020.1.26-32Test.; Trifonova E.A., Swarovskaya M.G., Ganzha O.A. et al. The interaction effect of angiogenesis and endothelial dysfunction-related gene variants increases the susceptibility of recurrent pregnancy loss. J Assist Reprod Genet. 2019;36(4):717-26. https://doi.org/10.1007/s10815-019-01403-2Test.; Zhao X., Li Q., Yu F. et al. Gene polymorphism associated with endothelial nitric oxide synthase (4VNTR, G894T, C786T) and unexplained recurrent spontaneous abortion risk: a meta-analysis. Medicine (Baltimore). 2019;98(4):e14175. https://doi.org/10.1097/MD.0000000000014175Test.; Cao X., Cui Y., Zhang X. et al. The correlation of sperm morphology with unexplained recurrent spontaneous abortion: a systematic review and meta-analysis. Oncotarget. 2017;8(33):55646-56. https://doi.org/10.18632/oncotarget.17233Test.; Carlini T., Paoli D., Pelloni M. et al. Sperm DNA fragmentation in Italian couples with recurrent pregnancy loss. Reprod Biomed Online. 2017;34(1):58-65. https://doi.org/10.1016/j.rbmo.2016.09.014Test.; Coughlan C., Clarke H., Cutting R. et al. Sperm DNA fragmentation, recurrent implantation failure and recurrent miscarriage. Asian J Androl. 2015;17(4):681-5. https://doi.org/10.4103/1008-682X.144946Test.; https://www.gynecology.su/jour/article/view/1035Test

  7. 7
    دورية أكاديمية

    المؤلفون: Kudryavtseva, V A, Vasileva, N V

    المصدر: IOP Conference Series: Earth and Environmental Science ; volume 751, issue 1, page 012100 ; ISSN 1755-1307 1755-1315

  8. 8
    دورية أكاديمية

    المؤلفون: Kudryavtseva, V A

    المصدر: IOP Conference Series: Earth and Environmental Science ; volume 751, issue 1, page 012027 ; ISSN 1755-1307 1755-1315

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    دورية أكاديمية

    المصدر: Siberian journal of oncology; Том 19, № 5 (2020); 131-144 ; Сибирский онкологический журнал; Том 19, № 5 (2020); 131-144 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2020-19-5

    وصف الملف: application/pdf

    العلاقة: https://www.siboncoj.ru/jour/article/view/1588/797Test; Smallridge R.C., Ain K.B., Asa S.L., Bible K.C., Brierley J.D., Burman K.D., Kebebew E., Lee N.Y., Nikiforov Y.E., Rosenthal M.S., Shah M.H., Shaha A.R., Tuttle R.M.; American Thyroid Association Anaplastic Thyroid Cancer Guidelines Taskforce. American Thyroid Association guidelines for management of patients with anaplastic thyroid cancer. Thyroid. 2012 Nov; 22(11): 1104–39. doi:10.1089/thy.2012.0302.; Giuffrida D., Gharib H. Anaplastic thyroid carcinoma: current diagnosis and treatment. Ann Oncol. 2000; 11(9): 1083–9. doi:10.1023/a:1008322002520.; Nikiforov Y.E., Nikiforova M.N. Molecular genetics and diagnosis of thyroid cancer. Nat Rev Endocrinol. 2011; 7(10): 569–80. doi:10.1038/ nrendo.2011.142.; Ahmed S., Ghazarian M.P., Cabanillas M.E., Zafereo M.E., Williams M.D., Vu T., Schomer D.F., Debnam J.M. Imaging of Anaplastic Thyroid Carcinoma. AJNR Am J Neuroradiol. 2018 Mar; 39(3): 547–551. doi:10.3174/ajnr.A5487.; Rao S.N., Zafereo M., Dadu R., Busaidy N.L., Hess K., Cote G.J., Williams M.D., William W.N., Sandulache V., Gross N., Gunn G.B., Lu C., Ferrarotto R., Lai S.Y., Cabanillas M.E. Patterns of Treatment Failure in Anaplastic Thyroid Carcinoma. Thyroid. 2017 May; 27(5): 672–681. doi:10.1089/thy.2016.0395.; FDA approves dabrafenib plus trametinib for anaplastic thyroid cancer with BRAF V600E mutation [Internet]. https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-dabrafenibplus-trametinib-anaplastic-thyroid-cancer-braf-v600e-mutationTest (cited 18.08.2020).; Subbiah V., Kreitman R.J., Wainberg Z.A., Cho J.Y., Schellens J.H.M., Soria J.C., Wen P.Y., Zielinski C., Cabanillas M.E., Urbanowitz G., Mookerjee B., Wang D., Rangwala F., Keam B. Dabrafenib and Trametinib Treatment in Patients With Locally Advanced or Metastatic BRAF V600- Mutant Anaplastic Thyroid Cancer. J Clin Oncol. 2018 Jan 1; 36(1): 7–13. doi:10.1200/JCO.2017.73.6785.; Пылев А.Л., Жандарова А.А., Петров К.С., Романов Д.С., Лисовой В.А., Голуб С.В. Анапластический рак щитовидной железы. Есть ли свет в конце туннеля? Опухоли головы и шеи. 2020; 10(1): 10–19.; Ciarallo A., Marcus C., Taghipour M., Subramaniam R.M. Value of Fluorodeoxyglucose PET/Computed Tomography Patient Management and Outcomes in Thyroid Cancer. PET Clin. 2015 Apr; 10(2): 265–78. doi:10.1016/j.cpet.2014.12.009.; Santhanam P., Khthir R., Solnes L.B., Ladenson P.W. The relationship of braf.v600e mutation status to fdg pet/ct avidity in thyroid cancer: a review and meta-analysis. Endocr Pract. 2018; 24(1): 21–26. doi:10.4158/EP-2017-0080.; Landa I., Ibrahimpasic T., Boucai L., Sinha R., Knauf J.A., Shah R.H., Dogan S., Ricarte-Filho J.C., Krishnamoorthy G.P., Xu B., Schultz N., Berger M.F., Sander C., Taylor B.S., Ghossein R., Ganly I., Fagin J.A. Genomic and transcriptomic hallmarks of poorly differentiated and anaplastic thyroid cancers. J Clin Invest. 2016 Mar 1; 126(3): 1052–66. doi:10.1172/JCI85271.; Quiros R.M., Ding H.G., Gattuso P., Prinz R.A., Xu X. Evidence that one subset of anaplastic thyroid carcinomas are derived from papillary carcinomas due to BRAF and p53 mutations. Cancer. 2005; 103(11): 2261–8. doi:10.1002/cncr.21073.; Lim A.M., Taylor G.R., Fellowes A., Cameron L., Lee B., Hicks R.J., McArthur G.A., Angel C., Solomon B., Rischin D. BRAF Inhibition in BRAFV600E-Positive Anaplastic Thyroid Carcinoma. J Natl Compr Canc Netw. 2016 Mar; 14(3): 249–54. doi:10.6004/jnccn.2016.0030.; Paraiso K.H., Fedorenko I.V., Cantini L.P., Munko A.C., Hall M., Sondak V.K., Messina J.L., Flaherty K.T., Smalley K.S. Recovery of phospho-ERK activity allows melanoma cells to escape from BRAF inhibitor therapy. Br J Cancer. 2010 Jun 8; 102(12): 1724–30. doi:10.1038/sj.bjc.6605714.; Flaherty K.T., Infante J.R., Daud A., Gonzalez R., Kefford R.F., Sosman J., Hamid O., Schuchter L., Cebon J., Ibrahim N., Kudchadkar R., Burris H.A.3rd, Falchook G., Algazi A., Lewis K., Long G.V., Puzanov I., Lebowitz P., Singh A., Little S., Sun P., Allred A., Ouellet D., Kim K.B., Patel K., Weber J. Combined BRAF and MEK inhibition in melanoma with BRAF V600 mutations. N Engl J Med. 2012 Nov 1; 367(18): 1694–703. doi:10.1056/NEJMoa1210093.; Cabanillas M.E., Ferrarotto R., Garden A.S., Ahmed S., Busaidy N.L., Dadu R., Williams M.D., Skinner H., Gunn G.B., Grosu H., Iyer P., Hofmann M.C., Zafereo M. Neoadjuvant BRAF- and Immune-Directed Therapy for Anaplastic Thyroid Carcinoma. Thyroid. 2018 Jul; 28(7): 945–951. doi:10.1089/thy.2018.0060.; Wang J.R., Zafereo M.E., Dadu R., Ferrarotto R., Busaidy N.L., Lu C., Ahmed S., Gule-Monroe M.K., Williams M.D., Sturgis E.M., Goepfert R.P., Gross N.D., Lai S.Y., Gunn G.B., Phan J., Rosenthal D.I., Fuller C.D., Morrison W.H., Iyer P., Cabanillas M.E. Complete Surgical Resection Following Neoadjuvant Dabrafenib Plus Trametinib in BRAFV600E-Mutated Anaplastic Thyroid Carcinoma. Thyroid. 2019 Aug; 29(8): 1036–43. doi:10.1089/thy.2019.0133.; Cabanillas M.E., Dadu R., Iyer P., Wanland K.B., Busaidy N.L., Ying A., Gule-Monroe M., Wang J.R., Zafereo M., Hofmann M.C. Acquired Secondary RAS Mutation in BRAFV600E-Mutated Thyroid Cancer Patients Treated with BRAF Inhibitors. Thyroid. 2020; 30(9): 1288–96. doi:10.1089/thy.2019.0514.; Midthun L., Shaheen S., Deisch J., Senthil M., Tsai J., Hsueh C.T. Concomitant KRAS and BRAF mutations in colorectal cancer. J Gastrointest Oncol. 2019 Jun; 10(3): 577–581. doi:10.21037/jgo.2019.01.10.; Abravanel D.L., Nishino M., Sholl L.M., Ambrogio C., Awad M.M. An Acquired NRAS Q61K Mutation in BRAF V600E-Mutant Lung Adenocarcinoma Resistant to Dabrafenib Plus Trametinib. J Thorac Oncol. 2018 Aug; 13(8): e131e133. doi:10.1016/j.jtho.2018.03.026.; Bunney P.E., Zink A.N., Holm A.A., Billington C.J., Kotz C.M. Orexin activation counteracts decreases in nonexercise activity thermogenesis (NEAT) caused by high-fat diet. Physiol Behav. 2017 Jul 1; 176: 139–48. doi:10.1016/j.physbeh.2017.03.040.; Bastman J.J., Serracino H.S., Zhu Y., Koenig M.R., Mateescu V., Sams S.B., French J.D. Tumor-Infiltrating T Cells and the PD-1 Checkpoint Pathway in Advanced Differentiated and Anaplastic Thyroid Cancer. J Clin Endocrinol Metab. 2016; 101(7): 2863–2873. doi:10.1210/jc.2015-4227.; Naing A., Gainor J.F., Gelderblom H., Forde P.M., Butler M.O., Lin C.C., Sharma S., Ochoa de Olza M., Varga A., Taylor M., Schellens J.H.M., Wu H., Sun H., Silva A.P., Faris J., Mataraza J., Cameron S., Bauer T.M. A first-in-human phase 1 dose escalation study of spartalizumab (PDR001), an anti-PD-1 antibody, in patients with advanced solid tumors. J Immunother Cancer. 2020 Mar; 8(1): e000530. doi:10.1136/jitc-2020-000530.; Capdevila J., Wirth L.J., Ernst T., Ponce Aix S., Lin C.C., Ramlau R., Butler M.O., Delord J.P., Gelderblom H., Ascierto P.A., Fasolo A., Führer D., Hütter-Krönke M.L., Forde P.M., Wrona A., Santoro A., Sadow P.M., Szpakowski S., Wu H., Bostel G., Faris J., Cameron S, Varga A., Taylor M. PD-1 Blockade in Anaplastic Thyroid Carcinoma. J Clin Oncol. 2020 Aug 10; 38(23): 2620–2627. doi:10.1200/JCO.19.02727.; https://www.siboncoj.ru/jour/article/view/1588Test

  10. 10
    دورية أكاديمية

    المصدر: Obstetrics, Gynecology and Reproduction; Vol 14, No 4 (2020); 449-456 ; Акушерство, Гинекология и Репродукция; Vol 14, No 4 (2020); 449-456 ; 2500-3194 ; 2313-7347

    وصف الملف: application/pdf

    العلاقة: https://www.gynecology.su/jour/article/view/793/833Test; ISUOG Guidelines. Sonographic examination of the fetal central nervous system: guidelines for performing the 'basic examination' and the 'fetal neurosonogram'. Ultrasound Obstet Gynecol. 2007;29:109–16. https://doi.org/10.1002/uog.3909Test.; Демикова Н.С., Подольская М.А., Лапина А.С., Асанов А.Ю. Влияние пренатальной диагностики и селективных прерываний беременности на частоту врожденных пороков развития. Акушерство и гинекология. 2017;(7):130–5. https://doi.org/10.18565/aig.2017.7.130-5Test.; Симаходский А.С., Романенко О.П. Эффективность диагностики и лечения врожденных пороков развития в Санкт-Петербурге за 2006-2015 гг. Российский педиатрический журнал. 2017;20(4):214–7. https://doi.org/10.18821/1560-9561-2017-20-4-214-217Test.; Морозова Е.А., Сергеева Р.Р., Морозов Д.В. Современные проблемы диагностики и лечения неонатальных судорог. Эпилепсия и пароксизмальные состояния. 2018;10(4):17–25. https://doi.org/10.17749/2077-8333.2018.10.4.017-025Test.; Заваденко А.Н., Медведев М.И., Дегтярева М.Г. и др. Причины неонатальных судорог у детей различного гестационного возраста. Эпилепсия и пароксизмальные состояния. 2018;10(3):19–30. https://doi.org/10.17749/2077-8333.2018.10.3.019-030Test.; Кожанова Т.В., Жилина С.С., Мещерякова Т.И. и др. Мутация в гене ALD H7A1 у пациента с пиридоксин-зависимой неонатальной эпилептической энцефалопатией: клинический случай. Эпилепсия и пароксизмальные состояния. 2019;11(1):70–8. https://doi.org/10.17749/2077-8333.2019.11.1.70-78Test.; Huang J., Wah I.Y.M., Pooh R.K., Choy K.W. Molecular genetics in fetal neurology. Semin Fetal Neonatal Med. 2012;17(6):341–6. https://doi.org/10.1016/j.siny.2012.07.007Test.; Petracchi F., Crespo L., Michia C. et al. Holoprosencephaly at prenatal diagnosis: analysis of 28 cases regarding etiopathogenic diagnoses. Prenat Diagn. 2011;31(9):887–91. https://doi.org/10.1002/pd.2796Test.; Goetzinger K.R., Stamilio D.M., Dicke J.M., Macones G.A. Evaluating the incidence and likelihood ratios for chromosomal abnormalities in fetuses with common central nervous system malformations. Am J Obstet Gynecol. 2008;199(3):285.e1–6. https://doi.org/10.1016/j.ajog.2008.06.100Test.; Evangelidou P., Sismani C., Ioannides M. et al. Clinical application of whole-genome array CGH during prenatal diagnosis: study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations. Mol Cytogenet. 2010;3:24. https://doi.org/10.1186/1755-8166-3-24Test.; Гинтер Е.К., Золотухина Т.В., Антоненко В.Г. и др. Цитогенетические методы диагностики хромосомных болезней: Методическое пособие для врачей. М.: РМАПО-МГНЦ, 2009. 82 с.; Wapner R.J., Martin C.L., Levy B. et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med. 2012;367(23):2175–84. https://doi.org/10.1056/NEJMoa1203382Test.; Bui T-H., Vetro A., Zuffardi O., Shaffer L.G. Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era? Prenat Diagn. 2011;31(3):235–43. https://doi.org/10.1002/pd.2722Test.; Friedman J.M. High-resolution array genomic hybridization in prenatal diagnosis. Prenat Diagn. 2009;29(1):20–8. https://doi.org/10.1002/pd.2129Test.; Vestergaard E.M., Christensen R., Petersen O.B., Vogel I. Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings. Acta Obstet Gynecol Scand. 2013;92(7):762–8. https://doi.org/10.1111/aogs.12146Test.; Киевская Ю.К., Шилова Н.В., Канивец И.В. и др. Применение хромосомного микроматричного анализа для диагностики хромосомной патологии у плодов с врожденными пороками сердца. Уральский медицинский журнал. 2019;(15):18–22. https://doi.org/10.25694/URMJ.2019.15.06Test.; D'Amours G., Kibar Z., Mathonnet G. et al. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype. Clin Genet. 2012;81(2):128–41. https://doi.org/10.1111/j.1399-0004.2011.01687Test.; Kearney H.M., Thorland E.C., Brown K.K. et al.; Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genet Med. 2011;13(7):680–5. https://doi.org/10.1097/GIM.0b013e3182217a3aTest; Sun L., Wu Q., Jiang S-W. et al. Prenatal diagnosis of central nervous system anomalies by high-resolution chromosomal microarray analysis. Biomed Res Int. 2015;2015:426379. https://doi.org/10.1155/2015/426379Test.; Wapner R.J., Martin C.L., Levy B. et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. New Engl J Med. 2012;367(23): 2175–84. https://doi.org/10.1056/NEJMoa1203382Test.; https://www.gynecology.su/jour/article/view/793Test