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Journal Abstract Search

173 related items for PubMed ID: 15633165

  • 21. Partial trisomy of chromosome 6q: an interstitial duplication of the long arm.
    Zneimer SM, Ziel B, Bachman R.
    Am J Med Genet; 1998 Nov 02; 80(2):133-5. PubMed ID: 9805129
    [Abstract] [Full Text] [Related]

  • 22. Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.
    Demori E, Devescovi R, Benussi DG, Dolce S, Carrozzi M, Villa N, Miertus J, Amoroso A, Pecile V.
    Am J Med Genet A; 2004 Oct 15; 130A(3):288-94. PubMed ID: 15378554
    [Abstract] [Full Text] [Related]

  • 23. Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications.
    Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L.
    Am J Med Genet A; 2005 Oct 01; 138A(2):175-80. PubMed ID: 16152635
    [Abstract] [Full Text] [Related]

  • 24. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP, Kleczkowska A, Kenis H, Decock P, Van den Berghe H.
    Ann Genet; 1989 Oct 01; 32(3):174-6. PubMed ID: 2573314
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. Partial tetrasomy 15 due to a unique inverted triplication of chromosome15q24-q26.
    James PA, Aftimos S, Oei P.
    Am J Med Genet A; 2004 Oct 01; 130A(2):208-10. PubMed ID: 15372521
    [No Abstract] [Full Text] [Related]

  • 27. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
    Bhat M, Morrison PJ, Getty A, McManus D, Tubman R, Nevin NC.
    Am J Med Genet; 2000 Mar 20; 91(3):201-3. PubMed ID: 10756343
    [Abstract] [Full Text] [Related]

  • 28. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.
    Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M.
    Am J Med Genet A; 2004 Sep 01; 129A(3):261-4. PubMed ID: 15326625
    [Abstract] [Full Text] [Related]

  • 29. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 01; 32(3):346-9. PubMed ID: 2729354
    [Abstract] [Full Text] [Related]

  • 30. Partial trisomy for short arm of chromosome 5.
    Yasutomo K, Suzue T, Nishioka A, Kozan H, Sekiguchi T, Ohara K, Okamoto T, Iwai T, Endo S.
    Acta Paediatr Jpn; 1993 Aug 01; 35(4):336-9. PubMed ID: 8379327
    [Abstract] [Full Text] [Related]

  • 31. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG, Schuil J, Van Raveswaaij-Arts C, De Pater JM.
    Genet Couns; 2004 Aug 01; 15(4):405-10. PubMed ID: 15658615
    [Abstract] [Full Text] [Related]

  • 32. Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3).
    Kleczkowska A, Fryns JP, Moerman P, Vandenberghe K, Van den Berghe H.
    Clin Genet; 1987 Jul 01; 32(1):49-56. PubMed ID: 3621654
    [Abstract] [Full Text] [Related]

  • 33. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL, Van Dyke DL, Wiktor A, Walker H, Feldman GL.
    Am J Med Genet; 1993 Dec 01; 47(8):1198-201. PubMed ID: 8291556
    [Abstract] [Full Text] [Related]

  • 34. FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
    Dierlamm J, Wlodarska I, Michaux L, Vermeesch JR, Meeus P, Stul M, Criel A, Verhoef G, Thomas J, Delannoy A, Louwagie A, Cassiman JJ, Mecucci C, Hagemeijer A, Van den Berghe H.
    Genes Chromosomes Cancer; 1997 Oct 01; 20(2):155-66. PubMed ID: 9331566
    [Abstract] [Full Text] [Related]

  • 35. Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.
    Tzschach A, Krause-Plonka I, Menzel C, Knoblauch A, Toennies H, Hoeltzenbein M, Radke M, Ropers HH, Kalscheuer V.
    Am J Med Genet A; 2006 May 15; 140(10):1108-10. PubMed ID: 16619204
    [Abstract] [Full Text] [Related]

  • 36. Duplication 20p identified via fluorescent in situ hybridization.
    LeChien KA, McPherson E, Estop AM.
    Am J Med Genet; 1994 Apr 01; 50(2):187-9. PubMed ID: 7516625
    [Abstract] [Full Text] [Related]

  • 37. Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13.
    Mehra S, Christ L, Jeng L, Zinn AB, Schwartz S.
    Am J Med Genet A; 2005 Aug 30; 137(2):217-21. PubMed ID: 16059944
    [Abstract] [Full Text] [Related]

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