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Journal Abstract Search

169 related items for PubMed ID: 8775421

  • 1. Telomeric translocations are uncommon.
    Rivera H, Sitch FL, Crolla JA.
    Genet Couns; 1995; 6(4):343-7. PubMed ID: 8775421
    [Abstract] [Full Text] [Related]

  • 2. Frequency of chromosome healing and interstitial telomeres in 40 cases of constitutional abnormalities.
    Fortin F, Beaulieu Bergeron M, Fetni R, Lemieux N.
    Cytogenet Genome Res; 2009; 125(3):176-85. PubMed ID: 19738378
    [Abstract] [Full Text] [Related]

  • 3. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
    Ballif BC, Wakui K, Gajecka M, Shaffer LG.
    Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
    [Abstract] [Full Text] [Related]

  • 4. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
    Mignon-Ravix C, Depetris D, Luciani JJ, Cuoco C, Krajewska-Walasek M, Missirian C, Collignon P, Delobel B, Croquette MF, Moncla A, Kroisel PM, Mattei MG.
    Eur J Hum Genet; 2007 Apr; 15(4):432-40. PubMed ID: 17264869
    [Abstract] [Full Text] [Related]

  • 5. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP.
    Genet Couns; 1998 Apr; 9(3):215-21. PubMed ID: 9777345
    [Abstract] [Full Text] [Related]

  • 6. FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.
    Ballif BC, Kashork CD, Shaffer LG.
    Eur J Hum Genet; 2000 Oct; 8(10):764-70. PubMed ID: 11039576
    [Abstract] [Full Text] [Related]

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  • 8. Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.
    Sismani C, Armour JA, Flint J, Girgalli C, Regan R, Patsalis PC.
    Eur J Hum Genet; 2001 Jul; 9(7):527-32. PubMed ID: 11464244
    [Abstract] [Full Text] [Related]

  • 9. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
    Alves C, Carvalho F, Cremades N, Sousa M, Barros A.
    Eur J Hum Genet; 2002 Aug; 10(8):467-74. PubMed ID: 12111641
    [Abstract] [Full Text] [Related]

  • 10. Pathogenesis of jumping translocations: a molecular cytogenetics study.
    Wan TS, Ma SK, Chow EY, Li YH, Lin SY, Chan LC.
    Leuk Res; 2004 Oct; 28(10):1075-9. PubMed ID: 15289020
    [Abstract] [Full Text] [Related]

  • 11. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S.
    Rev Invest Clin; 1996 Oct; 48(1):27-33. PubMed ID: 8815483
    [Abstract] [Full Text] [Related]

  • 12. Nonreciprocal and jumping translocations of 15q1----qter in Prader-Willi syndrome.
    Rivera H, Zuffardi O, Gargantini L.
    Am J Med Genet; 1990 Nov; 37(3):311-7. PubMed ID: 2260556
    [Abstract] [Full Text] [Related]

  • 13. Fluorescence in situ hybridization of rDNA, telomeric (TTAGGG)n and (GATA)n repeats in the red abalone Haliotis rufescens (Archaeogastropoda: Haliotidae).
    Gallardo-Escárate C, Alvarez-Borrego J, del Río-Portilla MA, Cross I, Merlo A, Rebordinos L.
    Hereditas; 2005 Feb; 142(2005):73-9. PubMed ID: 16970615
    [Abstract] [Full Text] [Related]

  • 14. Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.
    Schleiermacher G, Bourdeaut F, Combaret V, Picrron G, Raynal V, Aurias A, Ribeiro A, Janoueix-Lerosey I, Delattre O.
    Oncogene; 2005 May 05; 24(20):3377-84. PubMed ID: 15735707
    [Abstract] [Full Text] [Related]

  • 15. Jumping translocations.
    Berger R, Bernard OA.
    Genes Chromosomes Cancer; 2007 Aug 05; 46(8):717-23. PubMed ID: 17444494
    [Abstract] [Full Text] [Related]

  • 16. Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.
    Ravnan JB, Tepperberg JH, Papenhausen P, Lamb AN, Hedrick J, Eash D, Ledbetter DH, Martin CL.
    J Med Genet; 2006 Jun 05; 43(6):478-89. PubMed ID: 16199540
    [Abstract] [Full Text] [Related]

  • 17. Interstitial telomeric sequences at the junction site of a jumping translocation.
    Vermeesch JR, Petit P, Speleman F, Devriendt K, Fryns JP, Marynen P.
    Hum Genet; 1997 Jun 05; 99(6):735-7. PubMed ID: 9187665
    [Abstract] [Full Text] [Related]

  • 18. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
    Panasiuk B, Usinskiené R, Kostyk E, Rybałko A, Stasiewicz-Jarocka B, Krzykwa B, Pieńkowska-Grela B, Kucinskas V, Michalova K, Midro AT.
    Ann Genet; 2004 Jun 05; 47(1):11-28. PubMed ID: 15050871
    [Abstract] [Full Text] [Related]

  • 19. Distribution of telomeric (TTAGGG)(n) sequences in avian chromosomes.
    Nanda I, Schrama D, Feichtinger W, Haaf T, Schartl M, Schmid M.
    Chromosoma; 2002 Nov 05; 111(4):215-27. PubMed ID: 12424522
    [Abstract] [Full Text] [Related]

  • 20. Effect of bleomycin on interstitial telomeric sequences of immortalized Chinese hamster ovary cells.
    Sánchez J, Bianchi MS, Bolzán AD.
    Mutat Res; 2009 Oct 02; 669(1-2):139-46. PubMed ID: 19540250
    [Abstract] [Full Text] [Related]

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