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153 related items for PubMed ID: 15704122

  • 1. Prenatal diagnosis of trisomy 1q21-qter: case report and review of literature.
    Machlitt A, Kuepferling P, Bommer C, Koerner H, Chaoui R.
    Am J Med Genet A; 2005 Apr 15; 134A(2):207-11. PubMed ID: 15704122
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
    Sifakis S, Eleftheriades M, Kappou D, Murru R, Konstantinidou A, Orru S, Ziegler M, Liehr T, Manolakos E, Papoulidis I.
    Birth Defects Res A Clin Mol Teratol; 2014 Apr 15; 100(4):284-93. PubMed ID: 24677675
    [Abstract] [Full Text] [Related]

  • 3. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.
    Karaoguz MY, Biri A, Pala E, Kan D, Poyraz A, Kurdoglu M, Percin EF.
    Genet Couns; 2006 Apr 15; 17(2):197-204. PubMed ID: 16970038
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of de novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born.
    Fernández-Novoa MC, Vargas MT, Granell MR, Carreto P.
    Prenat Diagn; 2004 Jun 15; 24(6):414-7. PubMed ID: 15229838
    [Abstract] [Full Text] [Related]

  • 5. Distal partial trisomy 1q: report of two cases and a review of the literature.
    Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T.
    Prenat Diagn; 2007 Sep 15; 27(9):865-71. PubMed ID: 17605151
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y, Yakut T, Egelí U, Ozerkan K.
    Prenat Diagn; 2002 Nov 15; 22(11):957-61. PubMed ID: 12424755
    [Abstract] [Full Text] [Related]

  • 7. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
    Duba HC, Erdel M, Löffler J, Bereuther L, Fischer H, Utermann B, Utermann G.
    J Med Genet; 1997 Apr 15; 34(4):309-13. PubMed ID: 9138155
    [Abstract] [Full Text] [Related]

  • 8. Partial trisomy of the long arm of chromosome 1: prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature.
    Cambosu F, Capobianco G, Fogu G, Bandiera P, Pirino A, Moro MA, Sanna R, Soro G, Dessole M, Montella A.
    J Obstet Gynaecol Res; 2013 Feb 15; 39(2):592-7. PubMed ID: 22925348
    [Abstract] [Full Text] [Related]

  • 9. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W.
    Prenat Diagn; 2006 Apr 15; 26(4):313-20. PubMed ID: 16506269
    [Abstract] [Full Text] [Related]

  • 10. First case of trisomy 13 plus mosaic trisomy 1q.
    Liehr T, Schmidt M, Starke H, Ziegler M, Kittner G, Heller A, Rubtsov N, Trifonov V, Claussen U.
    Fetal Diagn Ther; 2002 Apr 15; 17(3):133-6. PubMed ID: 11914563
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 13. Double autosomal trisomy (1q21.2----qter and 14pter----q13) in a female fetus with nuchal oedema.
    Fryns JP, Kleczkowska A, Moerman P, van den Berghe K, van den Berghe H.
    Ann Genet; 1987 Jun 16; 30(4):240-2. PubMed ID: 3501268
    [Abstract] [Full Text] [Related]

  • 14. Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1q.
    Bartsch C, Aslan M, Köhler J, Miny P, Horst J, Holzgreve W, Rehder H, Fritz B.
    Fetal Diagn Ther; 2001 Jun 16; 16(5):265-73. PubMed ID: 11509847
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
    [Abstract] [Full Text] [Related]

  • 16. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W.
    Prenat Diagn; 2005 Feb 01; 25(2):112-8. PubMed ID: 15712324
    [Abstract] [Full Text] [Related]

  • 17. De novo 1q32q44 duplication and distal 1q trisomy syndrome.
    Nowaczyk MJ, Bayani J, Freeman V, Watts J, Squire J, Xu J.
    Am J Med Genet A; 2003 Jul 15; 120A(2):229-33. PubMed ID: 12833404
    [Abstract] [Full Text] [Related]

  • 18. Pure duplication 1q41-qter: further delineation of trisomy 1q syndromes.
    Kulikowski LD, Bellucco FT, Nogueira SI, Christofolini DM, Smith Mde A, de Mello CB, Brunoni D, Melaragno MI.
    Am J Med Genet A; 2008 Oct 15; 146A(20):2663-7. PubMed ID: 18798309
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis of a recombinant chromosome 7 resulting in trisomy 7q11.22 --> qter.
    Tchirikov M, Merinsky A, Strohner M, Bonin M, Beyer V, Haaf T, Bartsch O.
    Am J Med Genet A; 2010 Mar 15; 152A(3):721-5. PubMed ID: 20186810
    [Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of complete sole trisomy 1q.
    Pettenati MJ, Berry M, Shashi V, Hartley Bowen J, Harper M.
    Prenat Diagn; 2001 Jun 15; 21(6):435-40. PubMed ID: 11438944
    [Abstract] [Full Text] [Related]

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