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Journal Abstract Search

540 related items for PubMed ID: 17369689

  • 21. 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; 49(5):431-8. PubMed ID: 16497571
    [Abstract] [Full Text] [Related]

  • 22. Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.
    Vranova V, Mentzlova D, Oltova A, Linkova V, Zezulkova D, Filkova H, Mendelova D, Sterba J, Kuglik P.
    Neoplasma; 2008; 55(1):23-30. PubMed ID: 18190236
    [Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of 2q32 deletion syndrome characterized by multiple segmental deletions and complex chromosomal rearrangement involving chromosomes 2, 5 and 7.
    Thorson HL, Surti U, Sathanoori M, Kochmar SJ, Torchia B, Rajkovic A.
    Fetal Diagn Ther; 2012; 31(3):196-200. PubMed ID: 22415219
    [Abstract] [Full Text] [Related]

  • 24. Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24.
    Hernando C, Plaja A, Català V, Sarret E, Egozcue J, Fuster C.
    Fertil Steril; 2004 Dec; 82(6):1666-71. PubMed ID: 15589876
    [Abstract] [Full Text] [Related]

  • 25. A rare case of de novo distal 19q trisomy prenatally diagnosed.
    Rombout S, Sartenaer D, Parmentier B, Dugauquier C, Gillerot Y.
    Prenat Diagn; 2004 Oct; 24(10):822-7. PubMed ID: 15503276
    [Abstract] [Full Text] [Related]

  • 26. [Molecular cytogenetic analysis for a familial complex chromosomal rearrangement].
    Qian WP, Tan YQ, Tjia WM, Song D, Guan XY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):302-4. PubMed ID: 15952121
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  • 27. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
    Gibson LH, McGrath J, Yang-Feng TL.
    Am J Med Genet; 1997 Feb 11; 68(4):417-20. PubMed ID: 9021014
    [Abstract] [Full Text] [Related]

  • 28. Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis.
    Park TS, Song J, Lee KA, Min YH, Lee SG, Park Y, Kim J, Lee EY, Choi JR.
    Cancer Genet Cytogenet; 2008 May 11; 183(1):72-6. PubMed ID: 18474302
    [Abstract] [Full Text] [Related]

  • 29. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
    Darnaude MT, Diaz de Bustamante A, Cabello P, Vallcorba I.
    Ann Genet; 1996 May 11; 39(2):61-3. PubMed ID: 8766134
    [Abstract] [Full Text] [Related]

  • 30. [Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].
    Li L, Zhou XY, Ji XQ, Yang YQ, Cao L, Zhou J, Liu A, Cheng J, Liu Y, Hu P, Xu ZF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr 11; 29(2):214-7. PubMed ID: 22487837
    [Abstract] [Full Text] [Related]

  • 31. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE, Shim SH, Mark HF, Huang XL, Milunsky JM.
    Exp Mol Pathol; 2006 Jun 11; 80(3):262-6. PubMed ID: 16516886
    [Abstract] [Full Text] [Related]

  • 32. Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.
    Huang B, Solomon S, Thangavelu M, Peters K, Bhatt S.
    Prenat Diagn; 2006 Dec 11; 26(12):1142-50. PubMed ID: 17009345
    [Abstract] [Full Text] [Related]

  • 33. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.
    Liehr T.
    Methods Mol Biol; 2008 Dec 11; 444():27-38. PubMed ID: 18425469
    [Abstract] [Full Text] [Related]

  • 34. Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus.
    Palka C, Alfonsi M, Morizio E, Soranno A, La Rovere D, Matarrelli B, Rullo AL, Zori R, Chiarelli F, Calabrese G.
    Eur J Med Genet; 2011 Dec 11; 54(3):333-6. PubMed ID: 21354345
    [Abstract] [Full Text] [Related]

  • 35. Cytogenetical diagnosis in paraffin-embedded fetoplacental tissue using comparative genomic hybridization.
    Ozcan T, Burki N, Parkash V, Huang X, Pejovic T, Mahoney MJ, Ward DC.
    Prenat Diagn; 2000 Jan 11; 20(1):41-4. PubMed ID: 10701850
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  • 36. A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male.
    Ergul E, Liehr T, Mrasek K, Sazci A.
    Fertil Steril; 2009 Jul 11; 92(1):391.e9-391.e12. PubMed ID: 19368909
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  • 37. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
    Curotti G, Benkhalifa M, Raybaud C, Picard F, Bellec V, Qumsiyeh MB.
    Genet Couns; 1999 Jul 11; 10(3):259-64. PubMed ID: 10546097
    [Abstract] [Full Text] [Related]

  • 38. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].
    Balícek P, Jüttnerová V, Jarosová M, Fialová J, Fiedler Z, Kolmanová J.
    Cas Lek Cesk; 2001 Mar 01; 140(4):122-4. PubMed ID: 11284430
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  • 39. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.
    Prenat Diagn; 2006 Mar 01; 26(3):206-13. PubMed ID: 16450348
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  • 40. 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 01; 25(6):492-6. PubMed ID: 15966044
    [Abstract] [Full Text] [Related]

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