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Journal Abstract Search

402 related items for PubMed ID: 9777345

  • 1. 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; 9(3):215-21. PubMed ID: 9777345
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  • 2. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
    Canún S, Mutchinick O, Shaffer LG, Fernández C.
    Am J Med Genet; 1998 Nov 16; 80(3):199-203. PubMed ID: 9843037
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  • 3. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.
    Prenat Diagn; 2006 Mar 16; 26(3):206-13. PubMed ID: 16450348
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  • 6. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A, Bova R, Bellanova G, Chindemi A, Zappata S, Brahe C.
    Am J Med Genet; 1997 Aug 08; 71(2):139-43. PubMed ID: 9217211
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  • 9. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM.
    Genet Couns; 2007 Aug 08; 18(1):29-48. PubMed ID: 17515299
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  • 10. Fusion of 9 beta-satellite and telomere (TTAGGG)n sequences results in a jumping translocation.
    Reddy KS, Murphy T.
    Hum Genet; 2000 Sep 08; 107(3):268-75. PubMed ID: 11071389
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  • 11. Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.
    Wyandt HE, Lebo RV, Fenerci EY, Sadhu DN, Milunsky JM.
    Am J Med Genet; 2000 Aug 14; 93(4):305-12. PubMed ID: 10946358
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  • 12. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT, Qumsiyeh MB, Martens PR, Tharapel SA, Dalton JD, Ward JC, Wilroy RS.
    Am J Med Genet; 1991 Jul 01; 40(1):117-20. PubMed ID: 1887840
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  • 13. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W.
    Genet Couns; 2006 Jul 01; 17(1):57-63. PubMed ID: 16719278
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  • 14. Specific subtelomere loss on chromosome der(11)t(3;11)(q23;q23)x2 in anaplastic thyroid cancer cell line OCUT-1.
    Kammori M, Onoda N, Nakamura K, Izumiyama N, Ogisawa K, Kurabayashi R, Ogawa T, Kaminishi M, Poon SS, Takubo K.
    Int J Mol Med; 2006 Jul 01; 18(1):9-16. PubMed ID: 16786150
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  • 15. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T, van den Berghe L, Smeets E, Fryns JP.
    Ann Genet; 1999 Jul 01; 42(4):215-20. PubMed ID: 10674161
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  • 20. Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
    Kulikowski LD, Christ LA, Nogueira SI, Brunoni D, Schwartz S, Melaragno MI.
    Am J Med Genet A; 2006 Jan 01; 140(1):82-7. PubMed ID: 16333825
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