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301 related items for PubMed ID: 15065104

  • 1. Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation.
    Migliori MV, Pettinari A, Ciaschini AM, Piermattei P, Pigliapoco F, Discepoli G.
    Prenat Diagn; 2004 Apr; 24(4):290-2. PubMed ID: 15065104
    [Abstract] [Full Text] [Related]

  • 2. [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
    [Abstract] [Full Text] [Related]

  • 3. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
    Wang H, McLaughlin M, Thompson C, Hunter AG.
    Am J Med Genet; 1993 Jun 15; 46(5):559-62. PubMed ID: 8322821
    [Abstract] [Full Text] [Related]

  • 4. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
    Phelan MC, Blackburn W, Rogers RC, Crawford EC, Cooley NR, Schrock E, Ning Y, Ried T.
    Prenat Diagn; 1998 Nov 15; 18(11):1174-80. PubMed ID: 9854728
    [Abstract] [Full Text] [Related]

  • 5. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
    Peschka B, Leygraaf J, Hansmann D, Hansmann M, Schröck E, Ried T, Engels H, Schwanitz G, Schubert R.
    Prenat Diagn; 1999 Dec 15; 19(12):1143-9. PubMed ID: 10590433
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP, Devriendt K, Chern SR, Lee CC, Wang W, Lin SP.
    Prenat Diagn; 2000 May 15; 20(5):384-9. PubMed ID: 10820405
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
    Giardino D, Corti C, Ballarati L, Finelli P, Valtorta C, Botta G, Giudici M, Grosso E, Larizza L.
    Prenat Diagn; 2006 Jun 15; 26(6):565-70. PubMed ID: 16683274
    [Abstract] [Full Text] [Related]

  • 8. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG, Spikes AS, Macha M, Dunn R.
    J Reprod Med; 1996 May 15; 41(5):367-71. PubMed ID: 8725766
    [Abstract] [Full Text] [Related]

  • 9. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.
    In Vivo; 2006 May 15; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 10. 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 May 15; 49(5):431-8. PubMed ID: 16497571
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of del(9)(p24): a sex reverse case.
    Privitera O, Vessecchia G, Bernasconi B, Bettio D, Stioui S, Giordano G.
    Prenat Diagn; 2005 Oct 15; 25(10):945-8. PubMed ID: 16086437
    [Abstract] [Full Text] [Related]

  • 12. Detection of translocations involving the Y-chromosome in prospective prenatal screening of common chromosomal aneuploidies by FISH.
    Verlinsky Y, Ginsberg N, Chmura M, White M, Strom C, Kuliev A.
    Prenat Diagn; 1998 Apr 15; 18(4):390-2. PubMed ID: 9602488
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
    Santolaya-Forgas J, De Leon J, Powell WC, Tonk V.
    Prenat Diagn; 2004 Mar 15; 24(3):209-12. PubMed ID: 15057955
    [Abstract] [Full Text] [Related]

  • 14. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
    Mercier S, Fellmann F, Cattin J, Bresson JL.
    Prenat Diagn; 1996 Nov 15; 16(11):1046-50. PubMed ID: 8953640
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of del(4)(q27q31.23), due to a maternal balanced complex chromosome rearrangement, characterized by array-CGH.
    Malvestiti F, De Toffol S, Chinetti S, Grimi B, Favero G, Borsatti A, Maggi F, Simoni G, Romana Grati F.
    Prenat Diagn; 2010 Mar 15; 30(3):280-3. PubMed ID: 20049850
    [No Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 15; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.
    Chen CP, Lin CC, Su YN, Tsai FJ, Chen JT, Chern SR, Lee CC, Town DD, Chen LF, Wu PC, Wang W.
    Taiwan J Obstet Gynecol; 2010 Jun 15; 49(2):188-91. PubMed ID: 20708526
    [Abstract] [Full Text] [Related]

  • 18. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
    Hoffman DJ, Punnett HH, Pyeritz RE.
    Am J Perinatol; 2004 Feb 15; 21(2):69-71. PubMed ID: 15017469
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.
    Nataf V, Senat MV, Albert M, Bidat L, de Mazancourt P, Roume J, Allard L, Le Tessier D, Ville Y, Selva J.
    Prenat Diagn; 2002 Aug 15; 22(8):675-80. PubMed ID: 12210575
    [Abstract] [Full Text] [Related]

  • 20. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K, Tanemura M, Oya N, Suzumori N, Kim KC, Ohashi H, Fukushima Y.
    Prenat Diagn; 1998 Jul 15; 18(7):725-30. PubMed ID: 9706655
    [Abstract] [Full Text] [Related]

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