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Journal Abstract Search

130 related items for PubMed ID: 16110194

  • 21. Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22).
    Balci S, Engiz O, Yilmaz Z, Baltaci V.
    Genet Couns; 2006; 17(3):281-9. PubMed ID: 17100195
    [Abstract] [Full Text] [Related]

  • 22. [Therapy-related acute promyelocytic leukemia with a t(9;22)(q34;q11) and t(15;17)(q22;q11 to approximately 12) subclone].
    Mochiduki Y, Muramoto S.
    Rinsho Ketsueki; 2005 Nov; 46(11):1218-22. PubMed ID: 16440807
    [Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings.
    Aslan H, Karaman B, Yildirim G, Ceylan Y.
    Prenat Diagn; 2005 Nov; 25(11):1024-7. PubMed ID: 16231308
    [Abstract] [Full Text] [Related]

  • 24. Molecular cytogenetic characterization of a familial balanced reciprocal translocation t(11;18) (q13.3; q23) associated with pregnancy wastage.
    Liu JY, Wang XR, Zeng XL, Zhang CS, Hao S, Song YC.
    Cytogenet Genome Res; 2003 Nov; 103(1-2):8-13. PubMed ID: 15004456
    [Abstract] [Full Text] [Related]

  • 25. A Case of Complex Chromosome Translocation: 46, XY, t(4; 10; 13) (q31; q23; q12).
    Wang K, Zhao X, Tu H, Lin H.
    Clin Lab; 2019 Nov 01; 65(11):. PubMed ID: 31710435
    [Abstract] [Full Text] [Related]

  • 26. Using BAC clones to characterize unbalanced chromosome abnormalities in interphase cells.
    Plastira K, Maher E, Fantes J, Ramsay J, Angelopoulou R.
    Eur J Med Genet; 2006 Nov 01; 49(3):235-46. PubMed ID: 16762825
    [Abstract] [Full Text] [Related]

  • 27. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M, Przełozna B, Płodzien M, Bugno M, Wnuk M, Kotylak Z, Słota E.
    J Appl Genet; 2005 Nov 01; 46(4):419-21. PubMed ID: 16278518
    [Abstract] [Full Text] [Related]

  • 28. An aggressive Ewing sarcoma associated with a new variant translocation, t(4;11;22)(q25;q24;q12), hyperdiploid karyotype, and tetrasomy 8.
    Abdelmoula NB, Landman-Parker J, Tourniaire B, Josset P, Boccon-Gibod L, Peter M, Delattre O, Perot C, Taillemite JL, Portnoi MF, Van den Akker J.
    Cancer Genet Cytogenet; 2005 Dec 01; 163(2):186-8. PubMed ID: 16337867
    [No Abstract] [Full Text] [Related]

  • 29. High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).
    Wieland I, Muschke P, Volleth M, Röpke A, Pelz AF, Stumm M, Wieacker P.
    Genes Chromosomes Cancer; 2006 Oct 01; 45(10):945-9. PubMed ID: 16845657
    [Abstract] [Full Text] [Related]

  • 30. Prenatal detection of deletion 6q13q15 in a complex karyotype.
    Yu M, Obringer AC, Fowler MH, Hummel M, Wenger SL.
    Prenat Diagn; 2005 Dec 01; 25(12):1084-7. PubMed ID: 16231325
    [Abstract] [Full Text] [Related]

  • 31. Isodicentric 20q- in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2).
    Li T, Xue Y, Zhang J, Chen S, Pan J, Wu Y, Wang Y, Shen J.
    Cancer Genet Cytogenet; 2008 Feb 01; 181(1):55-9. PubMed ID: 18262055
    [Abstract] [Full Text] [Related]

  • 32. [Genetic analysis of translocation of chromosome t(4;9) in a child with rare chromosome abnormality].
    Wang J, Liu YH, Li LF.
    Nan Fang Yi Ke Da Xue Xue Bao; 2006 Jun 01; 26(6):856-7. PubMed ID: 16793620
    [Abstract] [Full Text] [Related]

  • 33. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
    Santos M, Mrasek K, Rigola MA, Starke H, Liehr T, Fuster C.
    Fertil Steril; 2007 Oct 01; 88(4):969.e11-7. PubMed ID: 17451694
    [Abstract] [Full Text] [Related]

  • 34. Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.
    Manvelyan M, Riegel M, Santos M, Fuster C, Pellestor F, Mazaurik ML, Schulze B, Polityko A, Tittelbach H, Reising-Ackermann G, Belitz B, Hehr U, Kelbova C, Volleth M, Gödde E, Anderson J, Küpferling P, Köhler S, Duba HC, Dufke A, Aktas D, Martin T, Schreyer I, Ewers E, Reich D, Mrasek K, Weise A, Liehr T.
    Int J Mol Med; 2008 Jun 01; 21(6):705-14. PubMed ID: 18506363
    [Abstract] [Full Text] [Related]

  • 35. Chromosomal aberrations in oral solitary fibrous tumor.
    Manor E, Bodner L.
    Cancer Genet Cytogenet; 2007 Apr 15; 174(2):170-2. PubMed ID: 17452261
    [Abstract] [Full Text] [Related]

  • 36. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H, Giuliano F, Massol C, Bloch C, De Ricaud D, Lambert JC, Perelman S.
    Eur J Med Genet; 2006 Apr 15; 49(5):431-8. PubMed ID: 16497571
    [Abstract] [Full Text] [Related]

  • 37. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
    Ozkinay F, Kanit H, Onay H, Cogulu O, Gunduz C, Ercal D, Ozkinay C.
    Genet Couns; 2006 Apr 15; 17(3):315-20. PubMed ID: 17100200
    [Abstract] [Full Text] [Related]

  • 38. Cytogenetic and clinical studies of a male infant with disorder of sexual development: case report.
    Balkan M, Duran H, Onen A, Oral D, Isi H, Fidanboy M, Alp MN, Budak T.
    Fertil Steril; 2008 Nov 15; 90(5):2003.e13-6. PubMed ID: 18691707
    [Abstract] [Full Text] [Related]

  • 39. Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2).
    Takeuchi M, Katayama Y, Okamura A, Yamamoto K, Shimoyama M, Matsui T.
    Cancer Genet Cytogenet; 2007 Nov 15; 179(1):85-7. PubMed ID: 17981222
    [No Abstract] [Full Text] [Related]

  • 40. An unusual translocation between 12tel and 14q11 in a large kindred.
    Palanduz S, Ustek D, Karaman B, Oztürk S, Cefle K, Başaran S.
    Hereditas; 1998 Nov 15; 128(3):231-4. PubMed ID: 9760871
    [Abstract] [Full Text] [Related]

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