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594 related items for PubMed ID: 16683274

  • 1. 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; 26(6):565-70. PubMed ID: 16683274
    [Abstract] [Full Text] [Related]

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

  • 3. 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 Feb; 22(4):249-53. PubMed ID: 17369689
    [Abstract] [Full Text] [Related]

  • 4. 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; 19(12):1143-9. PubMed ID: 10590433
    [Abstract] [Full Text] [Related]

  • 5. 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; 18(11):1174-80. PubMed ID: 9854728
    [Abstract] [Full Text] [Related]

  • 6. 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; 16(11):1046-50. PubMed ID: 8953640
    [Abstract] [Full Text] [Related]

  • 7. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L, Recalcati MP, Bedeschi MF, Lalatta F, Valtorta C, Bellini M, Finelli P, Larizza L, Giardino D.
    Eur J Med Genet; 2009 Nov; 52(4):218-23. PubMed ID: 19236961
    [Abstract] [Full Text] [Related]

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

  • 9. 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 Nov; 17(3):371-9. PubMed ID: 17100206
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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]

  • 12. [Genetic analysis of a complex chromosome rearrangement involving two chromosomes and four breakpoints in an azoospermic man].
    Luo YQ, Shen M, Qian YL, Chen YL, Xu CM, Jin F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr 16; 26(2):200-2. PubMed ID: 19350516
    [Abstract] [Full Text] [Related]

  • 13. [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]

  • 14. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun 01; 25(6):451-5. PubMed ID: 15966060
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 22(5):1292-7. PubMed ID: 17283038
    [Abstract] [Full Text] [Related]

  • 16. De novo exceptional complex chromosomal rearrangement in a healthy fertile male: case report and review of the literature.
    Farra C, Singer S, Dufke A, Ashkar H, Monsef C, Awwad J.
    Fertil Steril; 2011 Nov 01; 96(5):1160-4. PubMed ID: 21851937
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 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 Nov 15; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 19. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
    Guilherme RS, Cernach MC, Sfakianakis TE, Takeno SS, Nardozza LM, Rossi C, Bhatt SS, Liehr T, Melaragno MI.
    Cytogenet Genome Res; 2013 Nov 15; 141(4):317-23. PubMed ID: 23817307
    [Abstract] [Full Text] [Related]

  • 20. [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 15; 22(3):302-4. PubMed ID: 15952121
    [Abstract] [Full Text] [Related]

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