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Material Type: Artigo
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Prenatal and fetal diagnosis of trisomy 18 after low‐risk cell‐free fetal DNA screening: A report of four casesSheehan, Elizabeth ; Bacon, Victoria ; Lascurain, Seth ; Stone, Julia ; Yatsenko, Svetlana ; Aarabi, Mahmoud ; Skvarca, Lauren B. ; Clemens, Michele ; Saller, DevereuxPrenatal diagnosis, 2023-01, Vol.43 (1), p.36-41 [Periódico revisado por pares]EnglandTexto completo disponível |
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Material Type: Artigo
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Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratoryPetersen, Andrea K. ; Cheung, Sau Wai ; Smith, Janice L. ; Bi, Weimin ; Ward, Patricia A. ; Peacock, Sandra ; Braxton, Alicia ; Van Den Veyver, Ignatia B. ; Breman, Amy M.American journal of obstetrics and gynecology, 2017-12, Vol.217 (6), p.691.e1-691.e6 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Prenatal Diagnosis of Sex Chromosome Abnormalities: The 8-Year Experience of a Single Medical CenterVaknin, Zvi ; Reish, Orit ; Ben-Ami, Ido ; Heyman, Eli ; Herman, Arie ; Maymon, RonFetal diagnosis and therapy, 2008-01, Vol.23 (1), p.76-81 [Periódico revisado por pares]Basel, Switzerland: KargerTexto completo disponível |
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Material Type: Artigo
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Second trimester maternal serum analytes in triploid pregnancies: correlation with phenotype and sex chromosome complementBenn, Peter A. ; Gainey, Andrea ; Ingardia, Charles J. ; Rodis, John F. ; Egan, James F. X.Prenatal diagnosis, 2001-08, Vol.21 (8), p.680-686 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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The value of single umbilical artery in the prediction of fetal aneuploidy: findings in 12,672 pregnant womenGranese, Roberta ; Coco, Claudio ; Jeanty, PhilippeUltrasound quarterly, 2007-06, Vol.23 (2), p.117-121 [Periódico revisado por pares]United StatesTexto completo disponível |
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Material Type: Artigo
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FREE BETA hCG SCREENING OF HYDROPIC AND NON-HYDROPIC TURNER SYNDROME PREGNANCIESLAUNDON, CAROLINE H. ; SPENCER, KEVIN ; MACRI, JAMES N. ; ANDERSON, ROBERT W. ; BUCHANAN, PHILIP D.Prenatal diagnosis, 1996-09, Vol.16 (9), p.853-856 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Non-invasive prenatal testing: ethical issues exploredDE JONG, Antina ; DONDORP, Wybo J ; DE DIE-SMULDERS, Christine E. M ; FRINTS, Suzanne G. M ; DE WERT, Guido M. W. REuropean journal of human genetics : EJHG, 2010-03, Vol.18 (3), p.272-277 [Periódico revisado por pares]Basingstoke: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcomeBedei, Ivonne ; Gloning, Karl‐Philipp ; Joyeux, Luc ; Meyer‐Wittkopf, Matthias ; Willner, Daria ; Krapp, Martin ; Scharf, Alexander ; Degenhardt, Jan ; Heling, Kai‐Sven ; Kozlowski, Peter ; Trautmann, Kathrin ; Jahns, Kai M. ; Geipel, Annegret ; Tekesin, Ismail ; Elsässer, Michael ; Wilhelm, Lucas ; Gottschalk, Ingo ; Baumüller, Jan‐Erik ; Birdir, Cahit ; Schröer, Andreas ; Zöllner, Felix ; Wolter, Aline ; Schenk, Johanna ; Gehrke, Tascha ; Spaeth, Alicia ; Axt‐Fliedner, RolandPrenatal diagnosis, 2023-02, Vol.43 (2), p.183-191 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypesGrati, Francesca Romana ; Barlocco, Andrea ; Grimi, Beatrice ; Milani, Silvia ; Frascoli, Giuditta ; Di Meco, Anna Maria ; Liuti, Rosaria ; Trotta, Anna ; Chinetti, Sara ; Dulcetti, Francesca ; Ruggeri, Anna Maria ; De Toffol, Simona ; Clementi, Maurizio ; Maggi, Federico ; Simoni, GiuseppeAmerican journal of medical genetics. Part A, 2010-06, Vol.152A (6), p.1434-1442 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Simplifying the Ultrasound Findings of the Major Fetal Chromosomal AneuploidiesLiau, Joy, MD, PhD ; Romine, Lorene, MD ; Korty, Lauren A., MS ; Chao, Cherng, MD, JD ; White, Katherine, RDMS ; Harmon, Sheena, MD ; Ho, Yoona, MSIV ; Hull, Andrew D., MD ; Pretorius, Dolores H., MDCurrent problems in diagnostic radiology, 2014-11, Vol.43 (6), p.300-316 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |