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Journal Abstract Search

79 related items for PubMed ID: 7747765

  • 21. Another previously described 21 monosomy case turns out to be an unbalanced translocation.
    West BR, Allen EF.
    Am J Med Genet; 1998 Feb 03; 75(4):438. PubMed ID: 9482655
    [No Abstract] [Full Text] [Related]

  • 22. 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 03; 26(3):206-13. PubMed ID: 16450348
    [Abstract] [Full Text] [Related]

  • 23. Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21.
    Hertz B, Brandt CA, Petersen MB, Pedersen S, König U, Strømkjaer H, Jensen PK.
    Clin Genet; 1993 Aug 03; 44(2):89-94. PubMed ID: 7506129
    [Abstract] [Full Text] [Related]

  • 24. Complete monosomy mosaic of chromosome 21: case report and review of literature.
    Toral-Lopez J, Gonzalez-Huerta LM, Cuevas-Covarrubias SA.
    Gene; 2012 Dec 01; 510(2):175-9. PubMed ID: 22985727
    [Abstract] [Full Text] [Related]

  • 25. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.
    Chin Med J (Engl); 2003 Sep 01; 116(9):1298-303. PubMed ID: 14527352
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. [Study of a familial insertional translocation involving chromosomes 1 and 7 by using fluorescence in situ hybridization].
    Tan Y, Li X, Li L, Lu G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun 16; 18(3):183-6. PubMed ID: 11402445
    [Abstract] [Full Text] [Related]

  • 28. Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.
    Phelan MC, Morton CC, Stevenson RE, Tanzi RE, Stewart GD, Watkins PC, Gusella JF, Amos JA.
    Am J Hum Genet; 1988 Oct 16; 43(4):511-9. PubMed ID: 2902789
    [Abstract] [Full Text] [Related]

  • 29. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration.
    Qiu H, Xue Y, Zhang J, Pan J, Dai H, Wu Y, Wang Y, Chen S, Wu D.
    Exp Hematol; 2008 Nov 16; 36(11):1487-95. PubMed ID: 18715689
    [Abstract] [Full Text] [Related]

  • 30. FISHing for acrocentric associations between chromosomes 14 and 21 in human oogenesis.
    Cheng EY, Naluai-Cecchini T.
    Am J Obstet Gynecol; 2004 Jun 16; 190(6):1781-5; discussion 1785-7. PubMed ID: 15284799
    [Abstract] [Full Text] [Related]

  • 31. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W.
    Genet Couns; 2006 Jun 16; 17(1):57-63. PubMed ID: 16719278
    [Abstract] [Full Text] [Related]

  • 32. Novel translocation t(3;11)(p21;q24) in multiple myeloma characterised by FISH.
    Smith A, de Lambert R, Robson L.
    Ann Genet; 1999 Jun 16; 42(4):221-4. PubMed ID: 10674162
    [Abstract] [Full Text] [Related]

  • 33. Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21.
    McGinniss MJ, Rosenberg C, Stetten G, Schinzel AA, Binkert F, Petersen MB, Kearns WG, Kazazian HH, Pearson PL, Antonarakis SE.
    Am J Med Genet; 1993 Jul 01; 46(6):647-51. PubMed ID: 8362906
    [Abstract] [Full Text] [Related]

  • 34. Application of fluorescence in situ hybridization in defining a complex t(9;21;22) Ph formation.
    Mancini M, Nanni M, Cedrone M, De Cuia MR, Rondinelli MB, Malagnino F, Alimena G.
    Haematologica; 1994 Jul 01; 79(6):536-9. PubMed ID: 7896212
    [Abstract] [Full Text] [Related]

  • 35. A case of chronic neutrophilic leukemia with novel chromosomal abnormalities.
    Sai P, Kalavar M, Raval M, Sipot CR, Steier W.
    Clin Adv Hematol Oncol; 2004 Aug 01; 2(8):543-5; discussion 545. PubMed ID: 16163234
    [No Abstract] [Full Text] [Related]

  • 36. 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]

  • 37. Physical findings in 21q22 deletion suggest critical region for 21q- phenotype in q22.
    Theodoropoulos DS, Cowan JM, Elias ER, Cole C.
    Am J Med Genet; 1995 Nov 06; 59(2):161-3. PubMed ID: 8588579
    [Abstract] [Full Text] [Related]

  • 38. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
    Szabó Gabriella P, Balogh E, Jakab Z, Germán P, Bodnár F, Kiss A, Telek B, Oláh E.
    Orv Hetil; 2002 Dec 15; 143(50):2775-9. PubMed ID: 12583317
    [Abstract] [Full Text] [Related]

  • 39. Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle.
    Robinson HM, Harrison CJ, Moorman AV, Chudoba I, Strefford JC.
    Genes Chromosomes Cancer; 2007 Apr 15; 46(4):318-26. PubMed ID: 17243167
    [Abstract] [Full Text] [Related]

  • 40. Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture.
    Bregant L, Gersak K, Veble A.
    Genet Couns; 2005 Apr 15; 16(1):59-63. PubMed ID: 15844780
    [Abstract] [Full Text] [Related]

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