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124 related items for PubMed ID: 16354979

  • 1. Prenatal diagnosis of trisomy 9.
    Nakagawa M, Hashimoto K, Ohira H, Hamanaka T, Ozaki M, Suehara N.
    Fetal Diagn Ther; 2006; 21(1):68-71. PubMed ID: 16354979
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  • 2. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
    Machado IN, Heinrich JK, Campanhol C, Rodrigues-Peres RM, Oliveira FM, Barini R.
    Genet Mol Res; 2010 Mar 16; 9(1):441-8. PubMed ID: 20391329
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  • 3. Prenatal diagnosis of nonmosaic trisomy 9 and related ultrasound findings at 11.7 weeks.
    Pinette MG, Pan Y, Chard R, Pinette SG, Blackstone J.
    J Matern Fetal Med; 1998 Mar 16; 7(1):48-50. PubMed ID: 9502671
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  • 5. Prenatal diagnosis of complete trisomy 19q.
    Babić I, Brajenović-Milić B, Petrović O, Mustać E, Kapović M.
    Prenat Diagn; 2007 Jul 16; 27(7):644-7. PubMed ID: 17437325
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  • 6. Dichorionic triamniotic triplet pregnancy with monozygotic twins discordant for trisomy 13 after preimplantation genetic screening: case report.
    Taylor DM, Thum MY, Abdalla H.
    Fertil Steril; 2008 Nov 16; 90(5):2017.e5-9. PubMed ID: 18402943
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  • 8. Prenatal diagnosis of complete trisomy 9: a case report and review of the literature.
    Kor-Anantakul O, Suwanrath C, Kanngurn S, Rujirabanjerd S, Suntharasaj T, Pinjaroen S.
    Am J Perinatol; 2006 Feb 16; 23(2):131-5. PubMed ID: 16506121
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  • 10. Ultrasound detection and perinatal outcome of fetal trisomies 21, 18 and 13 in the absence of a routine fetal anomaly scan or biochemical screening.
    Moran CJ, Tay JB, Morrison JJ.
    Ultrasound Obstet Gynecol; 2002 Nov 16; 20(5):482-5. PubMed ID: 12423486
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  • 12. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun 16; 25(6):492-6. PubMed ID: 15966044
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  • 15. [PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN].
    Stoyanova V, Nedeva N, Linev A, Ivanov H, Petrova P, Krushkov K, Stratieva V, Vachev T.
    Akush Ginekol (Sofiia); 2015 Jun 16; 54(3):43-7. PubMed ID: 26137780
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  • 18. Trisomy 20 mosaicism and nonmosaic trisomy 20: a report of 2 cases.
    Joó JG, Beke A, Tóth-Pál E, Hargitai B, Szigeti Z, Papp C, Papp Z.
    J Reprod Med; 2006 Mar 16; 51(3):209-12. PubMed ID: 16674019
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  • 19. Congenital perineal hernia in a fetus with trisomy 18.
    Steffensen TS, Opitz JM, Gilbert-Barness E.
    Fetal Pediatr Pathol; 2009 Mar 16; 28(2):95-9. PubMed ID: 19241240
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