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Aging and aneuploidy: evidence for the preferential involvement of the inactive X chromosomeAbruzzo, M.A. ; Mayer, M. ; Jacobs, P.A.Cytogenetic and genome research, 1985, Vol.39 (4), p.275-278 [Periódico revisado por pares]Basel, Switzerland: KargerSem texto completo |
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Etiology of nondisjunction in humansAbruzzo, Michael A. ; Hassold, Terry J.Environmental and molecular mutagenesis, 1995, Vol.25 (S2), p.38-47 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanySem texto completo |
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Mosaic Turner syndrome: cytogenetics versus FISHABULHASAN, S. J. ; TAYEL, S. M. ; AL-AWADI, S. A.Annals of human genetics, 1999-05, Vol.63 (3), p.199-206 [Periódico revisado por pares]Edinburgh, UK: Cambridge University PressTexto completo disponível |
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Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for fragile X syndromeAdir, Vardit ; Shahak, Elena ; Dar, Hanna ; Borochowitz, Zvi UGenetic testing, 2003-12, Vol.7 (4), p.345-346United StatesTexto completo disponível |
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Turner syndrome and 45,X/47,XXX mosaicismAkbas, E ; Mutluhan, H ; Savasoglu, K ; Soylemez, F ; Ozturk, I ; Yazici, GGenetic counseling, 2009-01, Vol.20 (2), p.141 [Periódico revisado por pares]SwitzerlandSem texto completo |
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Silencing XIST on the future active X: Searching human and bovine preimplantation embryos for the repressorAksit, Melis A ; Yu, Bo ; Roelen, Bernard A J ; Migeon, Barbara REuropean journal of human genetics : EJHG, 2024-04, Vol.32 (4), p.399-406 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Ullrich-turner syndrome in monozygotic twinsAl-Awadi, S. A. ; Cuschieri, A. ; Farag, T. I. ; Naguib, K. ; Teebi, A. S. ; Al-Othman, S. A. ; Bahig, A. H.American journal of medical genetics, 1983-08, Vol.15 (4), p.537-542New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Nearly a third of abnormalities found after first-trimester screening are different than expected:10-year experience from a single centerAlamillo, Christina M. L. ; Krantz, David ; Evans, Mark ; Fiddler, Morris ; Pergament, EugenePrenatal diagnosis, 2013-03, Vol.33 (3), p.251-256 [Periódico revisado por pares]England: Blackwell Publishing LtdTexto completo disponível |
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Cytological and epidemiological findings in trisomies 13, 18, and 21: England and Wales 2004-2009Alberman, Eva ; Mutton, David ; Morris, Joan K.American journal of medical genetics. Part A, 2012-05, Vol.158A (5), p.1145-1150 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidiesAllingham-Hawkins, Diane J. ; Chitayat, David ; Cirigliano, Vincenzo ; Summers, Anne ; Tokunaga, Jason ; Winsor, Elizabeth ; Chun, KathyGenetics in medicine, 2011-02, Vol.13 (2), p.140-147 [Periódico revisado por pares]United States: Elsevier IncSem texto completo |