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1 |
Material Type: Artigo
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A case of non-mosaic X trisomy (65,XXX) in a Thoroughbred mare confirmed by cytogenetic and molecular analysisCieslak, Jakub ; Mackowski, Mariusz ; Skrzetuska, Weronika ; Fidos-Tama, Ewa ; Siwinska, Natalia ; Szczerbal, IzabelaJournal of applied genetics, 2024, Vol.65 (2), p.395-398 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |
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Material Type: Artigo
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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombinationMacDonald, M. ; Hassold, T. ; Harvey, J. ; Wang, L.H. ; Morton, N.E. ; Jacobs, P.Human molecular genetics, 1994-08, Vol.3 (8), p.1365-1371 [Periódico revisado por pares]Oxford: Oxford University PressSem texto completo |
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3 |
Material Type: Artigo
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21Park, V M ; Bravo, R R ; Shulman, L PJournal of medical genetics, 1995-08, Vol.32 (8), p.650-653 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |
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4 |
Material Type: Artigo
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Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidyMüller, U ; Weber, J L ; Berry, P ; Kupke, K GJournal of medical genetics, 1993-07, Vol.30 (7), p.597-600 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |
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5 |
Material Type: Artigo
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Y-specific DNA sequences in male patients with 46,XX and 47,XXX karyotypesMüller, Ulrich ; Latt, Samuel A. ; Donlon, Timothy ; Opitz, John M.American journal of medical genetics, 1987-10, Vol.28 (2), p.393-401 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Diplospermy II indicated as the origin of a liveborn human triploid (69,XXX)Page, B M ; Robson, E B ; Cook, P J ; Sanger, R ; Watt, J LJournal of medical genetics, 1981-10, Vol.18 (5), p.386-389 [Periódico revisado por pares]England: BMJ Publishing Group LtdTexto completo disponível |
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Material Type: Artigo
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Non‐invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective studySotiriadis, Alexandros ; Papoulidis, Ioannis ; Siomou, Elisavet ; Papageorgiou, Elena ; Eleftheriades, Makarios ; Papadopoulos, Vasilios ; Alexiou, Maria ; Manolakos, Emmanouil ; Athanasiadis, ApostolosPrenatal diagnosis, 2017-06, Vol.37 (6), p.583-592 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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Genetic diagnosis of sex chromosome aberrations in horses based on parentage test by microsatellite DNA and analysis of X- and Y-linked markersKakoi, H ; Hirota, K ; Gawahara, H ; Kurosawa, M ; Kuwajima, MEquine veterinary journal, 2005-03, Vol.37 (2), p.143-147 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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9 |
Material Type: Artigo
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Noninvasive Prenatal Screening Based on Second-Trimester Ultrasonographic Soft Markers in Low-Risk Pregnant WomenLiu, Yunyun ; Jing, Xiaosha ; Xing, Lingling ; Liu, Sha ; Liu, Jianlong ; Cheng, Jing ; Deng, Cechuan ; Bai, Ting ; Xia, Tianyu ; Wei, Xiang ; Luo, Yuan ; Zhou, Quanfang ; Zhu, Qian ; Liu, HongqianFrontiers in genetics, 2021-12, Vol.12, p.793894-793894 [Periódico revisado por pares]Switzerland: Frontiers Media S.ATexto completo disponível |
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Material Type: Artigo
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Expanded Croatian 12 X-STR loci database with an overview of anomalous profilesMršić, Gordan ; Ozretić, Petar ; Crnjac, Josip ; Merkaš, Siniša ; Sukser, Viktorija ; Račić, Ivana ; Rožić, Sara ; Barbarić, Lucija ; Popović, Maja ; Korolija, MarinaForensic science international : genetics, 2018-05, Vol.34, p.249-256 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |