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174 related items for PubMed ID: 3499849

  • 1. Dissociation of tdic chromosomes: about a t(15;18)(p11;p11) leading to 18p monosomy.
    Garcia-Esquivel L, Rivera H, Sanchez-Corona J, Ramirez ML, Jimenez M, Cantú JM.
    Ann Genet; 1987; 30(2):94-7. PubMed ID: 3499849
    [Abstract] [Full Text] [Related]

  • 2. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
    Wang JC, Nemana L, Kou SY, Habibian R, Hajianpour MJ.
    Am J Med Genet; 1997 Sep 05; 71(4):463-6. PubMed ID: 9286456
    [Abstract] [Full Text] [Related]

  • 3. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
    Alkan M, Ramelli GP, Hirsiger H, Keser I, Remonda L, Bühler EM, Moser H.
    Genet Couns; 2002 Sep 05; 13(2):151-6. PubMed ID: 12150215
    [Abstract] [Full Text] [Related]

  • 4. Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation.
    Nazarenko SA, Ostroverkhova NV, Vasiljeva EO, Nazarenko LP, Puzyrev VP, Malet P, Nemtseva TA.
    Am J Med Genet; 1999 Jul 16; 85(2):179-82. PubMed ID: 10406673
    [Abstract] [Full Text] [Related]

  • 5. Partial monosomy 15q due to de novo t(15;22)(q15;p11).
    Mori MA, Rodriguez L, Pinel I, Casas JM, Diaz de Bustamante A, Martinez-Frias ML.
    Ann Genet; 1987 Jul 16; 30(4):246-8. PubMed ID: 3322163
    [Abstract] [Full Text] [Related]

  • 6. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G, Jauch A, Eggermann T, Hardwick R, Kirsch S, Schiebel K, Rappold G, Robson L, Smith A.
    Am J Med Genet; 2000 May 15; 92(2):101-6. PubMed ID: 10797432
    [Abstract] [Full Text] [Related]

  • 7. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT, Qumsiyeh MB, Martens PR, Tharapel SA, Dalton JD, Ward JC, Wilroy RS.
    Am J Med Genet; 1991 Jul 01; 40(1):117-20. PubMed ID: 1887840
    [Abstract] [Full Text] [Related]

  • 8. 18p monosomy with midline defects and a de novo satellite identified by FISH.
    Taine L, Goizet C, Wen ZQ, Chateil JF, Battin J, Saura R, Lacombe D.
    Ann Genet; 1997 Jul 01; 40(3):158-63. PubMed ID: 9401105
    [Abstract] [Full Text] [Related]

  • 9. De novo (15;21) unbalanced translocation of paternal origin in a girl with Prader-Willi syndrome.
    Cuoco C, Bicocchi MP, Granata D, Mezzano P, Serra G.
    Am J Med Genet; 1990 Sep 01; 37(1):62-4. PubMed ID: 2240045
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
    Prontera P, Aiello V, Toschi M, Turci A, Gruppioni R, Buldrini B, Zago S, Bonfatti A, Donti E, Calzolari E, Sensi A.
    Genet Couns; 2007 Sep 01; 18(3):309-15. PubMed ID: 18019372
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
    McGhee EM, Qu Y, Wohlferd MM, Goldberg JD, Norton ME, Cotter PD.
    Clin Genet; 2001 Apr 01; 59(4):274-8. PubMed ID: 11298684
    [Abstract] [Full Text] [Related]

  • 12. Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma.
    Kajii T, Tsukahara M, Fukushima Y, Hata A, Matsuo K, Kuroki Y.
    Ann Genet; 1985 Apr 01; 28(4):219-23. PubMed ID: 3879432
    [Abstract] [Full Text] [Related]

  • 13. Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p).
    Barbi G, Kennerknecht I, Klett C.
    Am J Med Genet; 1992 Jul 01; 43(4):722-5. PubMed ID: 1621764
    [Abstract] [Full Text] [Related]

  • 14. Use of chromosome painting for marker chromosome identification in two children with congenital disorders.
    Doco-Fenzy M, Navrocki B, Cornillet P, Sabouraud P, Robillard P, Gruson N, Gaillard D, Adnet JJ.
    Bull Assoc Anat (Nancy); 1994 Jun 01; 78(241):9-13. PubMed ID: 8086666
    [Abstract] [Full Text] [Related]

  • 15. A new case of monosomy for 17q25----qter due to a maternal translocation [t(3;17)(p12;q24)].
    Luke S, Bennett HS, Pitter JH, Verma RS.
    Ann Genet; 1992 Jun 01; 35(1):48-50. PubMed ID: 1610120
    [Abstract] [Full Text] [Related]

  • 16. A tdic(5;15)(p31;p11) chromosome showing variation for constriction in the centromeric regions in a patient with the cri du chat syndrome.
    Dewald GW, Boros SJ, Conroy MM, Dahl RJ, Spurbeck JL, Vitek HA.
    Cytogenet Cell Genet; 1979 Jun 01; 24(1):15-26. PubMed ID: 456039
    [Abstract] [Full Text] [Related]

  • 17. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
    Abeliovich D, Dagan J, Lerer I, Silberstein S, Katznelson MB, Frydman M.
    Am J Med Genet; 1996 Dec 02; 66(1):45-51. PubMed ID: 8957510
    [Abstract] [Full Text] [Related]

  • 18. Duplication 18p with mild influence on the phenotype.
    Johansson B, Mertens F, Palm L, Englesson I, Kristoffersson U.
    Am J Med Genet; 1988 Apr 02; 29(4):871-4. PubMed ID: 3400732
    [Abstract] [Full Text] [Related]

  • 19. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A, Bova R, Bellanova G, Chindemi A, Zappata S, Brahe C.
    Am J Med Genet; 1997 Aug 08; 71(2):139-43. PubMed ID: 9217211
    [Abstract] [Full Text] [Related]

  • 20. Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation.
    Cantu JM, Hernandez A, Plascencia L, Vaca G, Moller M, Rivera H.
    Ann Genet; 1980 Aug 08; 23(3):183-6. PubMed ID: 6448566
    [Abstract] [Full Text] [Related]

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