Littérature scientifique sur le sujet « "cytogenetic markers" »
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Articles de revues sur le sujet ""cytogenetic markers""
Willatt, L., et J. Shipley. « Human Cytogenetic Cancer Markers ». Journal of Medical Genetics 35, no 4 (1 avril 1998) : 350. http://dx.doi.org/10.1136/jmg.35.4.350-a.
Texte intégralFink, James M. « Human Cytogenetic Cancer Markers ». American Journal of Clinical Pathology 109, no 4 (1 avril 1998) : 489.1–489. http://dx.doi.org/10.1093/ajcp/109.4.489.
Texte intégralWaters, J. « Human Cytogenetic Cancer Markers ». Molecular Pathology 50, no 5 (1 octobre 1997) : 279. http://dx.doi.org/10.1136/mp.50.5.279-c.
Texte intégralFonatsch, Christa. « Cytogenetic markers in hematoproliferative disorders ». Blut 51, no 5 (novembre 1985) : 315–28. http://dx.doi.org/10.1007/bf00320042.
Texte intégralLozzio, C. B., L. Lyall et E. Bamberger. « Molecular Cytogenetic Characterization of Chromosome Markers ». Genetics in Medicine 1, no 2 (février 1999) : 68. http://dx.doi.org/10.1097/00125817-199901000-00108.
Texte intégralRahesh, Jasmin, Arham Siddiqui, Praveen Tumula et Rahul Chandra. « A rare case of mixed phenotype acute leukemia : acute myeloid leukemia to early T-cell precursor acute lymphoblastic leukemia transformation ». Southwest Respiratory and Critical Care Chronicles 10, no 44 (22 juillet 2022) : 45–47. http://dx.doi.org/10.12746/swrccc.v10i44.967.
Texte intégralStrand, Jacob J., Terra L. Lasho, Susan M. Schwager, Michelle M. Elliott, Chin-Yang Li et Ayalew Tefferi. « Cytogenetic Profile, JAK2V617F Mutational Status, and Response to Drug Therapy in Myelofibrosis with Myeloid Metaplasia. » Blood 106, no 11 (16 novembre 2005) : 2591. http://dx.doi.org/10.1182/blood.v106.11.2591.2591.
Texte intégralGoes, Caio Augusto Gomes, Sandro Natal Daniel, Lucas Henrique Piva, George Shigueki Yasui, Roberto Ferreira Artoni, Diogo Teruo Hashimoto, Fausto Foresti et Fabio Porto-Foresti. « Cytogenetic markers as a tool for characterization of hybrids of Astyanax Baird & ; Girard, 1854 and Hyphessobrycon Eigenmann, 1907 ». Comparative Cytogenetics 14, no 2 (27 mai 2020) : 231–42. http://dx.doi.org/10.3897/compcytogen.v14i2.49513.
Texte intégralGoes, Caio Augusto Gomes, Sandro Natal Daniel, Lucas Henrique Piva, George Shigueki Yasui, Roberto Ferreira Artoni, Diogo Teruo Hashimoto, Fausto Foresti et Fábio Porto-Foresti. « Corrigenda : Cytogenetic markers as a tool for characterization of hybrids of Astyanax Baird & ; Girard, 1854 and Hyphessobrycon Eigenmann, 1907. Comparative Cytogenetics 14(2) : 231–242. https://doi.org/10.3897/CompCytogen.v14i2.49513 ». Comparative Cytogenetics 14, no 4 (29 décembre 2020) : 639–43. http://dx.doi.org/10.3897/compcytogen.v14i4.56080.
Texte intégralMendoza, Mayra N., Terje Raudsepp, Manuel J. More, Gustavo A. Gutiérrez et F. Abel Ponce de León. « Cytogenetic Mapping of 35 New Markers in the Alpaca (Vicugna pacos) ». Genes 11, no 5 (8 mai 2020) : 522. http://dx.doi.org/10.3390/genes11050522.
Texte intégralThèses sur le sujet ""cytogenetic markers""
Taylor, Christopher. « Cytogenetic and molecular genetic markers for chromosome 6R of rye linked to CCN resistance / ». Title page, contents and summary only, 1996. http://web4.library.adelaide.edu.au/theses/09PH/09pht239.pdf.
Texte intégralEndrizzi, J. E., et R. Sherman. « Cytogenetic Analysis of Lf Marker Gene and Monotelodisome 12L ». College of Agriculture, University of Arizona (Tucson, AZ), 1986. http://hdl.handle.net/10150/219756.
Texte intégralMilenko, Kolarski. « Prenatalni ultrazvučni skrining drugog trimestra trudnoće u predikciji Daunovog sindroma ». Phd thesis, Univerzitet u Novom Sadu, Medicinski fakultet u Novom Sadu, 2016. http://www.cris.uns.ac.rs/record.jsf?recordId=100904&source=NDLTD&language=en.
Texte intégralINTRODUCTIONS Prenatal diagnostic procedure represent a set of methods and techniques with the aim to afirmate or eliminate the presence of Down’s syndrome and other congenital anomalies Can be non-invasive and invasive methods. Non-invasive methods (laboratory or ultrasonographic) have the aim to make possible the most valid assessment of the risk of presence of an affected fetus in the pregnancy, selected pregnancy for invasive diagnostics procedures and citogenetics analisseskariotipingfoeti. Down’s syndrome, aneuploidy with trisomy 21 chromosomal, is the most common chromosomal numerical aberration associated with mental retardation of children (IQ< 70). Children with Down’s syndrome have characteristic phenotypic appearance with high frequent congenital anomalies that preclude a normal life and are frequently the cause of their earlier death. AIM The aim of the four year long investigation was to confirm the importance of ultrasound screening by the analyses of the basic ultrasound parameters for the second trimester, the thickness of the nuchal fold and the length of the femur of the fetus in the prediction of Down’s syndrome and other chromosomal aberrations of the fetus, as well as to improve other existing ultrasonic screenings of the first and second trimester of pregnancy by ultrasonic examination and analyses of the cephalic index and intraorbital space and the length of the fronto-thalamic distance. MATERIAL AND METODS Retrospective investigation (2010. 2011) and prospective investigation (2012.2013) includes 4655 pregnant women. For all pregnant women the genetic investigation of the fetus was performed. A total of 68 were found with chromosomal aberrations, 38 with Down’s syndrome. The method of haphazard choice in retrospective study and in prospective study ultrasound markers are examined. In retrospective analyses of the nuchal fold (<6mm and the length of femur <0.6, that represent basic ultrasound screening of the second trimester and are analyzed as parametric signs of the second trimester, and are analyzed as parametric markers, and analyses of the circulation of fetal blood through ductus venosus of the fetus. In the retrospective study the length of the nuchal fold (>6mm in length, that represent a basic ultrasound screening of the second trimester, and are analyzed as parametric markers in the prediction of Down’s syndrome and other chromosomal aberrations. RESULTS AND DISCUSION Cytogenetic analyses revealed 66 (1, 49%) pathologic karyotypes and Down syndrome were present in 31 (0, 68%) cases. All pathologic karyotypes were obtained after ultrasound examinations of 4552 pregnant women. Ultrasound markers for period 14th-22nd GW were analyzed with descriptive statistical methods and importance of pregnancy in older women, thickness of nuchal fold and lengths frontal thalamic distance were proofed in case of Down syndrome. Femoral bone lengths, cephalic index and intraorbital distances were similar for both groups, normal and pathologic karyotypes. Student’s t test revealed statistical significance with p<0, 001 values for nuchal fold thickness, frontal thalamic distance and older ages.Three additional ultrasound markers (frontal thalamic distance, cephalic index, intraorbital distance) improve prediction of Down syndrome and other chromosomal aberrations between 14th and 22nd GW as well. Multifactorial logistic regressive analyses revealed 93% sensitivity with 7% false positive results. Corelation between nuchal fold thickness and frontal thalamic distance improve prenatal ultrasound screening sensitivity. Using both ultrasound and biochemical screening (triple test) is way to improve sensitivity of non invasive screening in prediction of Down syndrome and other chromosomal aberrations. CONCLUSIONS Importance of pregnant women ages and higher risk for Down syndrome and other chromosomal aberrations was proofed (p<0, 001).Importance of nuchal fold thickness above 6mm (p<0, 001) and shorter femoral bone marker in period from 14th to 22nd GW in prediction of Down syndrome and other chromosomal aberrations are proofed (p<0, 001). Hypothesses that frontal thalamic distance improve ultrasound screening sensitivity was proofed was proofed (p<0, 001) since it is significantly shorter in Down syndrome and other chromosomal aberrations in comparison with fetuses with normal karyotypes. Comparative analyses of frontothalamic distance, nuchal fold thickness and femoral bone length in period from 14th to 22nd GW can signifi cantly improve prenatal diagnostic testing in Down syndrome prediction. Correlation between frontothalamic distance and nuchal fold thickness improve ultrasound screening sensitivity on 93% that is proofed with multifactorial logistic regressive analyses. Significance of multidisciplinary approach is high in Down syndrome prediction. Cost-benefit: High sensitivity of non invasive prenatal screening in Down syndrome prediction reduces costs for families and government since it costs ten time less than cytogenetic analyses and risk with invasive procedures is avoided.
Ali, Niaz. « Molecular markers, cytogenetics and epigenetics to characterize wheat-Thinopyrum hybrid lines conferring wheat streak mosaic virus resistance ». Thesis, University of Leicester, 2012. http://hdl.handle.net/2381/10951.
Texte intégralAll-Ericsson, Charlotta. « Uveal melanoma : cytogenetics, molecular biology and tumor immunology / ». Stockholm, 2002. http://diss.kib.ki.se/2002/91-7349-278-7.
Texte intégralJean, Martine. « Genetic mapping of restorer genes for cytoplasmic male sterility in Brassica napus using DNA markers ». Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=40147.
Texte intégralAnhalt, Ulrike C. M. « Characterisation of the initial generations of recombinant inbred lines in perennial ryegrass (Lolium perenne L.) using molecular markers and cytogenetics ». Thesis, University of Leicester, 2009. http://hdl.handle.net/2381/7495.
Texte intégralBabwah, Andy Videsh. « Development and application of biotechnological tools in the major crop plant, Brassica napus ». Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=37867.
Texte intégralPrado, Fernanda Dotti do [UNESP]. « Caracterização citogenética e molecular das espécies pintado (Pseudoplatystoma corruscans), cachara (Pseudoplatystoma reticulatum) e seus híbridos utilizados na piscicultura brasileira ». Universidade Estadual Paulista (UNESP), 2010. http://hdl.handle.net/11449/92441.
Texte intégralFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
A hibridação artificial interespecífica de peixes é utilizada em diversos estabelecimentos voltados à piscicultura no país, com a finalidade de produzir indivíduos mais vantajosos e favoráveis para o cultivo. Porém, devido principalmente às dificuldades encontradas na identificação dos híbridos, esta prática pode determinar o surgimento de sérios problemas como a contaminação genética dos estoques de cultivo, a comercialização de produtos híbridos como espécies puras, a introdução de espécies exóticas e escapes de produtos de piscicultura para o ambiente natural e até eventos de introgressão genética e extinção das espécies nativas. Neste contexto, o presente trabalho teve por objetivo analisar geneticamente exemplares das linhagens parentais de Pseudoplatystoma corruscans (pintado) e Pseudoplatystoma reticulatum (cachara) e seus híbridos interespecíficos pintachara (macho de pintado x fêmea de cachara) e cachapinta (fêmea de cachara x macho de pintado), provenientes dos estoques de cultivo do CEPTAlICMBio, Pirassununga, SP, a fim de identificar e estabelecer marcadores genéticos para possibilitar sua identificação e diferenciação. Também foram analisadas geneticamente amostras de P. corruscans e P. reticulatum coletadas no Rio Paraguai, MS (bacia do Paraguai) e de P. corruscans capturados do rio Mogi- Guaçu, SP (bacia do Alto Paraná), a fim de identificar a possível ocorrência de híbridos entre estas espécies na natureza. As análises citogenéticas revelaram um número diploide de 2n=56 cromossomos para ambas as espécies parentais, com cariótipos caracterizados por cromossomos dos tipos 20m+12am+12st+12a e número fundamental (NF) igual a 100, indicando uma fórmula cariotípica conservada entre estas espécies. A análise dos padrões de heterocromatina pelo bandamento C revelou blocos heterocromáticos localizados nas porções...
Artificial interspecific hybridization of fish is used in various establishments linked to fish farming in the country, in order to produce individuais more advantageous and favorable for cultivation. However, due mainly to difficulties in the hybrid products identification, this practice may determine the onset of serious problems such as genetic contamination of the breeder stocks, marketing of hybrids as pure species, introduction of exotic species and escapes of farmed products to the natural environment and sometimes leading to events of genetic introgression and extinction of native species. In such context, the present study aimed to analyze genetically copies of the parental lines of Pseudoplatystoma corruscans (pintado) and Pseudoplatystoma reticulatum (cachara) and their interspecific hybrids pintachara (female of pintado x male of cachara) and cachapinta (female of cachara x male of pintado), from the stocks manteined in CEPTAlICMBio, Pirassununga, SP, in order to characterize and establish genetic markers to allow their identification and differentiation. Samples of P. corruscans and P. reticulatum collected in the Paraguay river, MS (Paraguay basin) and P. corruscans captured in Mogi-Guaçu river, SP (Alto Paraná basin), also were genetically analyzed in order to identify the possible occurrence of hybrids between these species in nature. The cytogenetic analysis revealed a diploid number of 2n = 56 chromosomes for both parental species with karyotypes characterized by the formula 20m+12am+12st+12a and fundamental number (NF) of 100, indicating a karyotypic formula conserved among these species. The analysis of the heterochromatin C-banding patterns revealed heterochromatic blocks located in the pericentromeric and terminal portions of some chromosomes, the NOR was sim pie and located in one chromosome pai r and 5S ribosomal genes located on two different subtelocentric... (Complete abstract click electronic access below)
Prado, Fernanda Dotti do. « Caracterização citogenética e molecular das espécies pintado (Pseudoplatystoma corruscans), cachara (Pseudoplatystoma reticulatum) e seus híbridos utilizados na piscicultura brasileira / ». Botucatu : [s.n.], 2010. http://hdl.handle.net/11449/92441.
Texte intégralBanca: José Augusto Senhorini
Banca: Celso Benites
Resumo: A hibridação artificial interespecífica de peixes é utilizada em diversos estabelecimentos voltados à piscicultura no país, com a finalidade de produzir indivíduos mais vantajosos e favoráveis para o cultivo. Porém, devido principalmente às dificuldades encontradas na identificação dos híbridos, esta prática pode determinar o surgimento de sérios problemas como a contaminação genética dos estoques de cultivo, a comercialização de produtos híbridos como espécies puras, a introdução de espécies exóticas e escapes de produtos de piscicultura para o ambiente natural e até eventos de introgressão genética e extinção das espécies nativas. Neste contexto, o presente trabalho teve por objetivo analisar geneticamente exemplares das linhagens parentais de Pseudoplatystoma corruscans (pintado) e Pseudoplatystoma reticulatum (cachara) e seus híbridos interespecíficos "pintachara" (macho de pintado x fêmea de cachara) e "cachapinta" (fêmea de cachara x macho de pintado), provenientes dos estoques de cultivo do CEPTAlICMBio, Pirassununga, SP, a fim de identificar e estabelecer marcadores genéticos para possibilitar sua identificação e diferenciação. Também foram analisadas geneticamente amostras de P. corruscans e P. reticulatum coletadas no Rio Paraguai, MS (bacia do Paraguai) e de P. corruscans capturados do rio Mogi- Guaçu, SP (bacia do Alto Paraná), a fim de identificar a possível ocorrência de híbridos entre estas espécies na natureza. As análises citogenéticas revelaram um número diploide de 2n=56 cromossomos para ambas as espécies parentais, com cariótipos caracterizados por cromossomos dos tipos 20m+12am+12st+12a e número fundamental (NF) igual a 100, indicando uma fórmula cariotípica conservada entre estas espécies. A análise dos padrões de heterocromatina pelo bandamento C revelou blocos heterocromáticos localizados nas porções... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: Artificial interspecific hybridization of fish is used in various establishments linked to fish farming in the country, in order to produce individuais more advantageous and favorable for cultivation. However, due mainly to difficulties in the hybrid products identification, this practice may determine the onset of serious problems such as genetic contamination of the breeder stocks, marketing of hybrids as pure species, introduction of exotic species and escapes of farmed products to the natural environment and sometimes leading to events of genetic introgression and extinction of native species. In such context, the present study aimed to analyze genetically copies of the parental lines of Pseudoplatystoma corruscans (pintado) and Pseudoplatystoma reticulatum (cachara) and their interspecific hybrids "pintachara" (female of pintado x male of cachara) and "cachapinta" (female of cachara x male of pintado), from the stocks manteined in CEPTAlICMBio, Pirassununga, SP, in order to characterize and establish genetic markers to allow their identification and differentiation. Samples of P. corruscans and P. reticulatum collected in the Paraguay river, MS (Paraguay basin) and P. corruscans captured in Mogi-Guaçu river, SP (Alto Paraná basin), also were genetically analyzed in order to identify the possible occurrence of hybrids between these species in nature. The cytogenetic analysis revealed a diploid number of 2n = 56 chromosomes for both parental species with karyotypes characterized by the formula 20m+12am+12st+12a and fundamental number (NF) of 100, indicating a karyotypic formula conserved among these species. The analysis of the heterochromatin C-banding patterns revealed heterochromatic blocks located in the pericentromeric and terminal portions of some chromosomes, the NOR was sim pie and located in one chromosome pai r and 5S ribosomal genes located on two different subtelocentric... (Complete abstract click electronic access below)
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Livres sur le sujet ""cytogenetic markers""
Wolman, Sandra R., et Stewart Sell, dir. Human Cytogenetic Cancer Markers. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9.
Texte intégralR, Wolman Sandra, et Sell Stewart 1935-, dir. Human cytogenetic cancer markers. Totowa, N.J : Humana Press, 1997.
Trouver le texte intégralA, Bridge Julia, dir. The cytogenetics of bone and soft tissue tumors. Austin : R.G. Landes, 1994.
Trouver le texte intégralJeffrey, Cossman, dir. Molecular genetics in cancer diagnosis. New York : Elsevier, 1990.
Trouver le texte intégralSmall supernumerary marker chromosomes (sSMC) : A guide for human geneticists and clinicians. Heidelberg : New York, 2012.
Trouver le texte intégralC, Wagener, et Neumann S, dir. Molecular diagnostics of cancer. Berlin : Springer-Verlag, 1993.
Trouver le texte intégralWolman, Sandra R., et Stewart Sell. Human Cytogenetic Cancer Markers. Humana Press, 2012.
Trouver le texte intégralWolman, Sandra R., et Stewart Sell. Human Cytogenetic Cancer Markers. Humana, 2011.
Trouver le texte intégralChapitres de livres sur le sujet ""cytogenetic markers""
Slovak, Marilyn L. « Breast Tumor Cytogenetic Markers ». Dans Human Cytogenetic Cancer Markers, 111–49. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_6.
Texte intégralWorsham, Maria J., S. David Nathanson, Min Lee et Sandra R. Wolman. « Cytogenetic Biomarkers in Skin Cancer ». Dans Human Cytogenetic Cancer Markers, 289–317. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_12.
Texte intégralWolman, Sandra R., Stewart Sell et Eric Wolman. « An Introduction to Cancer Markers and Cytogenetics ». Dans Human Cytogenetic Cancer Markers, 1–14. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_1.
Texte intégralBrothman, Arthur R., et Briana J. Williams. « Prostate Cancer ». Dans Human Cytogenetic Cancer Markers, 223–46. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_10.
Texte intégralBell, Daphne W., et Joseph R. Testa. « Chromosomes in Lung Cancer ». Dans Human Cytogenetic Cancer Markers, 247–87. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_11.
Texte intégralShapiro, Joan Rankin, et Adrienne C. Scheck. « Brain Tumors ». Dans Human Cytogenetic Cancer Markers, 319–68. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_13.
Texte intégralGrebe, Stefan K. G., Norman L. Eberhardt et Robert B. Jenkins. « Cytogenetic Abnormalities Associated with Endocrine Neoplasia ». Dans Human Cytogenetic Cancer Markers, 369–401. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_14.
Texte intégralGriffin, Constance A. « Pancreatic Exocrine Tumors ». Dans Human Cytogenetic Cancer Markers, 403–23. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_15.
Texte intégralBridge, Julia A. « Soft Tissue Sarcomas ». Dans Human Cytogenetic Cancer Markers, 425–59. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_16.
Texte intégralCannizzaro, Linda A. « Special Techniques in Cytogenetics ». Dans Human Cytogenetic Cancer Markers, 461–77. Totowa, NJ : Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4612-3952-9_17.
Texte intégralActes de conférences sur le sujet ""cytogenetic markers""
STAPULIONYTĖ, Asta, Skaistė BONDZINSKAITĖ, Monika STRAVINSKAITĖ, Raimondas ŠIUKŠTA, Ričardas TARAŠKEVIČIUS et Tatjana ČĖSNIENĖ. « SOIL GENOTOXICITY BIOMONITORING IN RECULTIVATED FACTORY AREA USING THE CYTOGENETIC AND MOLECULAR ASSAYS IN TWO PLANT TEST-SYSTEMS ». Dans RURAL DEVELOPMENT. Aleksandras Stulginskis University, 2018. http://dx.doi.org/10.15544/rd.2017.025.
Texte intégralRytenkova, O. I., et A. N. Volkov. « BIOCHEMICAL PARAMETERS OF BLOOD IN PREGNANT WOMEN NORMALLY AND WITH CHROMOSOMAL PATHOLOGY OF THE FETUS ». Dans I International Congress “The Latest Achievements of Medicine, Healthcare, and Health-Saving Technologies”. Kemerovo State University, 2023. http://dx.doi.org/10.21603/conferencearticle_63edabf15da447.93685177.
Texte intégral« Identification of univalent chromosomes in monosomic lines of the Gossypium hirsutum L. cotton type with the help of cytogenetic markers ». Dans Current Challenges in Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences Novosibirsk State University, 2019. http://dx.doi.org/10.18699/icg-plantgen2019-81.
Texte intégralBuslaev, V. Yu, A. V. Torgunakova, Irina Milentyeva, Lyubov Dyshlyuk et V. I. Minina. « POPYMORPHISM OF IMMUNE RESPONSE GENES AND LUNG CANCER RISK IN NON-SMOKING RESIDENTS OF KUZBASS ». Dans I International Congress “The Latest Achievements of Medicine, Healthcare, and Health-Saving Technologies”. Kemerovo State University, 2023. http://dx.doi.org/10.21603/-i-ic-17.
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