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Journal Abstract Search

221 related items for PubMed ID: 8862625

  • 1. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
    Ruiz C, Grubs RE, Jewett T, Cox-Jones K, Abruzzese E, Pettenati MJ, Rao PN.
    Am J Med Genet; 1996 Aug 23; 64(3):478-84. PubMed ID: 8862625
    [Abstract] [Full Text] [Related]

  • 2. Prenatally diagnosed balanced chromosome rearrangements: eight years' experience.
    Peng HH, Chao AS, Wang TH, Chang YL, Chang SD.
    J Reprod Med; 2006 Sep 23; 51(9):699-703. PubMed ID: 17039698
    [Abstract] [Full Text] [Related]

  • 3. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina-Neto JM.
    Genet Couns; 2004 Sep 23; 15(3):303-10. PubMed ID: 15517822
    [Abstract] [Full Text] [Related]

  • 4. 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 23; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangements.
    Cotter PD, Caggana M, Willner JP, Babu A, Desnick RJ.
    Am J Med Genet; 1996 Dec 11; 66(2):197-9. PubMed ID: 8958330
    [Abstract] [Full Text] [Related]

  • 6. 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 11; 26(6):565-70. PubMed ID: 16683274
    [Abstract] [Full Text] [Related]

  • 7. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
    Mechoso B, Vaglio A, Quadrelli A, Mark HF, Huang XL, Milunsky A, Quadrelli R.
    Fetal Diagn Ther; 2007 Jun 11; 22(4):249-53. PubMed ID: 17369689
    [Abstract] [Full Text] [Related]

  • 8. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP, Chern SR, Wu PC, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2009 Dec 11; 48(4):389-99. PubMed ID: 20045761
    [Abstract] [Full Text] [Related]

  • 9. Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.
    Chen CP, Chern SR, Wu PC, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2010 Mar 11; 49(1):62-8. PubMed ID: 20466295
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis of de novo X;autosome translocations.
    Abrams L, Cotter PD.
    Clin Genet; 2004 May 11; 65(5):423-8. PubMed ID: 15099352
    [Abstract] [Full Text] [Related]

  • 11. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
    Goumy C, Mihaescu M, Tchirkov A, Giollant M, Benier C, Francannet C, Jaffray JY, Geneix A, Vago P.
    Genet Couns; 2006 May 11; 17(3):371-9. PubMed ID: 17100206
    [Abstract] [Full Text] [Related]

  • 12. Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature.
    Hastings RJ, Nisbet DL, Waters K, Spencer T, Chitty LS.
    Prenat Diagn; 1999 May 11; 19(5):436-45. PubMed ID: 10360512
    [Abstract] [Full Text] [Related]

  • 13. Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report.
    Joly-Helas G, de La Rochebrochard C, Mousset-Siméon N, Moirot H, Tiercin C, Romana SP, Le Caignec C, Clavier B, Macé B, Rives N.
    Hum Reprod; 2007 May 11; 22(5):1292-7. PubMed ID: 17283038
    [Abstract] [Full Text] [Related]

  • 14. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
    Schluth-Bolard C, Delobel B, Sanlaville D, Boute O, Cuisset JM, Sukno S, Labalme A, Duban-Bedu B, Plessis G, Jaillard S, Dubourg C, Henry C, Lucas J, Odent S, Pasquier L, Copin H, Latour P, Cordier MP, Nadeau G, Till M, Edery P, Andrieux J.
    Eur J Med Genet; 2009 May 11; 52(5):291-6. PubMed ID: 19505601
    [Abstract] [Full Text] [Related]

  • 15. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
    Fryns JP, Kleczkowska A, Kenis H.
    Ann Genet; 1984 May 11; 27(1):62-4. PubMed ID: 6609678
    [Abstract] [Full Text] [Related]

  • 16. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.
    Michalski K, Rauer M, Williamson N, Perszyk A, Hoo JJ.
    Am J Med Genet; 1993 Apr 01; 46(1):88-94. PubMed ID: 8494036
    [Abstract] [Full Text] [Related]

  • 17. De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review.
    Batanian JR, Eswara MS.
    Am J Med Genet; 1998 Jun 16; 78(1):44-51. PubMed ID: 9637422
    [Abstract] [Full Text] [Related]

  • 18. 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 Jun 16; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA, Pai GS, Stetten G.
    Am J Med Genet; 1994 Nov 15; 53(3):255-63. PubMed ID: 7856662
    [Abstract] [Full Text] [Related]

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