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Material Type: Artigo
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False‐negative trisomy 18 non‐invasive prenatal test result due to 48,XXX,+18 placental mosaicismGao, Y. ; Stejskal, D. ; Jiang, F. ; Wang, W.Ultrasound in obstetrics & gynecology, 2014-04, Vol.43 (4), p.477-478 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre studyGruchy, Nicolas ; Blondeel, Eleonore ; Le Meur, Nathalie ; Joly-Hélas, Géraldine ; Chambon, Pascal ; Till, Marianne ; Herbaux, Martine ; Vigouroux-Castera, Adeline ; Coussement, Aurélie ; Lespinasse, James ; Amblard, Florence ; Jimenez Pocquet, Mélanie ; Lebel-Roy, Camille ; Carré-Pigeon, Frédérique ; Flori, Elisabeth ; Mugneret, Francine ; Jaillard, Sylvie ; Yardin, Catherine ; Harbuz, Radu ; Collonge-Rame, Marie-Agnès ; Vago, Philippe ; Valduga, Mylène ; Leporrier, Nathalie ; Vialard, FrançoisPrenatal diagnosis, 2016-06, Vol.36 (6), p.523-529 [Periódico revisado por pares]England: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Incidence of sex chromosome aneuploidy in a prenatal population: 27‐year longitudinal study in Northern ItalySamango‐Sprouse, C. A. ; Grati, F. R. ; Brooks, M. ; Hamzik, M. P. ; Khaksari, K. ; Gropman, A. ; Taylor, A. ; Malvestiti, F. ; Grimi, B. ; Liuti, R. ; Milani, S. ; Chinetti, S. ; Trotta, A. ; Agrati, C. ; Repetti, E. ; Martin, K. A.Ultrasound in obstetrics & gynecology, 2023-08, Vol.62 (2), p.266-272 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two casesvan Huizen, M. E. ; Knegt, A. C. ; Bijlsma, E. K. ; Bilardo, C. M.Prenatal diagnosis, 2004-12, Vol.24 (12), p.1020-1021 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40‐year‐old woman with a mosaic Turner's karyotype (45,X/47,XXX)Acharya, Ganesh ; Jonsrud, Chistoffer ; Van Der Hagen, CarlBirger ; Maltau, Jan MartinActa obstetricia et gynecologica Scandinavica, 2003-08, Vol.82 (8), p.773-774 [Periódico revisado por pares]Oxford, UK: Munksgaard International PublishersTexto completo disponível |
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Material Type: Artigo
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18Chen, Chih‐Ping ; Chern, Schu‐Rern ; Yeh, Li‐Fan ; Chen, Wen‐Lin ; Chen, Li‐Feng ; Wang, WayseenPrenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Serum screening in complete triploidy 69,XXXDormeier, A ; Küffer, E ; Schurz, B ; Egarter, CPrenatal diagnosis, 1996-06, Vol.16 (6), p.578 [Periódico revisado por pares]EnglandTexto completo disponível |
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Material Type: Artigo
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Inter-observer discrepancy in scoring signals on interphase fish with an X library probe illustrated in a case of 47, XXXRobson, Lisa ; Smith, ArabellaPrenatal diagnosis, 1995-12, Vol.15 (12), p.1193-1195 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdSem texto completo |
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Material Type: Artigo
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Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorionSchwartz, S. ; Raffel, L. J.Prenatal diagnosis, 1992-12, Vol.12 (12), p.1043-1046 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdSem texto completo |
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Material Type: Artigo
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45,X/46,XX/47,XXX phenotypeLebel, Robert Roger ; Elejalde, B. Rafael ; De Elejalde, Maria Mercedes ; Avila, TeresitaPrenatal diagnosis, 1993-12, Vol.13 (12), p.1165-1166 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdSem texto completo |