المؤلفون: He, F., Si, K., Li, R., Zha, D., Dong, J., Miao, L., Bie, S., Jiang, J.

المصدر: IEEE Transactions on Antennas and Propagation IEEE Trans. Antennas Propagat. Antennas and Propagation, IEEE Transactions on. 70(9):8643-8647 Sep, 2022

المؤلفون: Amelie Limburg, Xueqian Qian, Bernice Brechtefeld, Nina Hedemann, Inken Flörkemeier, Christoph Rogmans, Leticia Oliveira-Ferrer, Nicolai Maass, Norbert Arnold, Dirk O. Bauerschlag, Jörg Paul Weimer

المصدر: Biomedicines, Vol 12, Iss 6, p 1171 (2024)

مصطلحات موضوعية: ovarian cancer, FISH, aCGH, chromoanagenesis, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2227-9059/12/6/1171; https://doaj.org/toc/2227-9059

URL الوصول: https://doaj.org/article/8d8eff3e1e8741f2b322bb36731c4e4b

المؤلفون: Mohammadi, M., Farahi, F.

المصدر: IEEE Transactions on Biomedical Engineering IEEE Trans. Biomed. Eng. Biomedical Engineering, IEEE Transactions on. 66(3):682-688 Mar, 2019

المؤلفون: Kinjal Gajjar, Alpesh Patel, B I Patel, Shiva Chettiar, Devendrasinh Jhala

المصدر: Reproduction and Fertility, Vol 4, Iss 2, Pp 1-11 (2023)

مصطلحات موضوعية: array comparative genomic hybridization (acgh), chromosome, copy number variations (cnvs), microarray, recurrent pregnancy loss (rpl), Reproduction, QH471-489, Gynecology and obstetrics, RG1-991

وصف الملف: electronic resource

Relation: https://raf.bioscientifica.com/view/journals/raf/4/2/RAF-22-0092.xml; https://doaj.org/toc/2633-8386

URL الوصول: https://doaj.org/article/a846f996ea944d3ea29c5d73f7f950ad

المؤلفون: Vilardell Nogales, Mireia

المساهمون: University/Department: Universitat Pompeu Fabra. Departament de Ciències Experimentals i de la Salut

مرشدي الرسالة: Pérez Jurado, Luis Alberto

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: sindrome Williams-Beuren, aneusomias parciales, analisis trancriptomico, CNV, variacion en el numero de copias, fuentes de variabilidad, diseño experimental, PSV, aCGH, variantes paralogas de secuencia, matriz de hibridacion genomica comparada

وصف الملف: application/pdf

URL الوصول: http://www.tdx.cat/TDX-0209109-143618
http://hdl.handle.net/10803/7117

المؤلفون: Feodora Stipoljev, Maja Oroz, Ana Vičić

المصدر: Liječnički vjesnik, Vol 145, Iss Supp 1, Pp 256-263 (2023)

مصطلحات موضوعية: NEURORAZVOJNI POREMEĆAJI, ACGH, CJELOEKSOMSKO SEKVENCIRANJE, CJELOGENOMSKO SEKVENCIRANJE, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://hrcak.srce.hr/file/434062; https://doaj.org/toc/0024-3477; https://doaj.org/toc/1849-2177

URL الوصول: https://doaj.org/article/0f09f97f8cb34eff98d10239c3721a68

المؤلفون: Svetlana Magadeeva, Xueqian Qian, Nadine Korff, Inken Flörkemeier, Nina Hedemann, Christoph Rogmans, Michael Forster, Norbert Arnold, Nicolai Maass, Dirk O. Bauerschlag, Jörg P. Weimer

المصدر: International Journal of Molecular Sciences, Vol 24, Iss 24, p 17467 (2023)

مصطلحات موضوعية: ovarian cancer, HRD, PARP-inhibitor, aCGH, genomic scars, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/24/24/17467; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/fdc7e9c5dd0944aeba619a6ce87f533b

المؤلفون: Pantou, Amelia^{Aff1, Aff2}, Mitrakos, Anastasios^{Aff1, Aff2, IDs10815022024619_cor2}, Kokkali, Georgia, Petroutsou, Konstantina, Tounta, Georgia, Lazaros, Leandros, Dimopoulos, Alexandros^{Aff4, Aff5}, Sfakianoudis, Konstantinos, Pantos, Konstantinos, Koutsilieris, Michael, Mavrou, Ariadni, Kanavakis, Emmanuel, Tzetis, Maria

المصدر: Journal of Assisted Reproduction and Genetics: An Official Journal of the American Society for Reproductive Medicine. 39(6):1341-1349

المؤلفون: Anna Repczynska, Katarzyna Julga, Jolanta Skalska-Sadowska, Magdalena M. Kacprzak, Alicja Bartoszewska-Kubiak, Ewelina Lazarczyk, Damian Loska, Malgorzata Drozniewska, Kamila Czerska, Jacek Wachowiak, Olga Haus

المصدر: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)

مصطلحات موضوعية: Fanconi anemia, Thrombocytopenia, Chromosome breakage test, aCGH, FANCA gene, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/84c419063b4f47a8888957f21c0aac58

المؤلفون: Türkyılmaz A, Geckinli BB, Tekin E, Ates EA, Yarali O, Cebi AH, Arman A

المصدر: Balkan Journal of Medical Genetics, Vol 24, Iss 2, Pp 15-24 (2022)

مصطلحات موضوعية: array-based comparative genomic hybridization (acgh), copy number variations (cnv), developmental delay, dysmorphic facial features, genotype-phenotype correlation, intellectual disability, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/b4c8addd46594dddad739bcf0d55ca5e