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Journal Abstract Search

139 related items for PubMed ID: 15832308

  • 1. BAC-based PCR fragment microarray: high-resolution detection of chromosomal deletion and duplication breakpoints.
    Ren H, Francis W, Boys A, Chueh AC, Wong N, La P, Wong LH, Ryan J, Slater HR, Choo KH.
    Hum Mutat; 2005 May; 25(5):476-82. PubMed ID: 15832308
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  • 2. BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH).
    Ylstra B, van den Ijssel P, Carvalho B, Brakenhoff RH, Meijer GA.
    Nucleic Acids Res; 2006 May; 34(2):445-50. PubMed ID: 16439806
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  • 3. Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high-resolution microarray comparative genomic hybridization.
    Weiss MM, Snijders AM, Kuipers EJ, Ylstra B, Pinkel D, Meuwissen SG, van Diest PJ, Albertson DG, Meijer GA.
    J Pathol; 2003 Jul; 200(3):320-6. PubMed ID: 12845628
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  • 6. Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays.
    Cai WW, Mao JH, Chow CW, Damani S, Balmain A, Bradley A.
    Nat Biotechnol; 2002 Apr; 20(4):393-6. PubMed ID: 11923847
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  • 8. Human and mouse oligonucleotide-based array CGH.
    van den Ijssel P, Tijssen M, Chin SF, Eijk P, Carvalho B, Hopmans E, Holstege H, Bangarusamy DK, Jonkers J, Meijer GA, Caldas C, Ylstra B.
    Nucleic Acids Res; 2005 Dec 16; 33(22):e192. PubMed ID: 16361265
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  • 9. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
    Hermsen MA, Tijssen M, Acero IH, Meijer GA, Ylstra B, Toral JF.
    Eur J Med Genet; 2005 Dec 16; 48(3):310-8. PubMed ID: 16179226
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  • 10. Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray.
    Ekong R, Jeremiah S, Judah D, Lehmann O, Mirzayans F, Hung YC, Walter MA, Bhattacharya S, Gant TW, Povey S, Wolfe J.
    Hum Mutat; 2004 Jul 16; 24(1):76-85. PubMed ID: 15221791
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  • 11. Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH.
    Guillaud-Bataille M, Valent A, Soularue P, Perot C, Inda MM, Receveur A, Smaïli S, Roest Crollius H, Bénard J, Bernheim A, Gidrol X, Danglot G.
    Nucleic Acids Res; 2004 Jul 29; 32(13):e112. PubMed ID: 15284333
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  • 12. Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms.
    Zhang ZF, Ruivenkamp C, Staaf J, Zhu H, Barbaro M, Petillo D, Khoo SK, Borg A, Fan YS, Schoumans J.
    Eur J Hum Genet; 2008 Jul 29; 16(7):786-92. PubMed ID: 18285835
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  • 13. DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones.
    Fiegler H, Carr P, Douglas EJ, Burford DC, Hunt S, Scott CE, Smith J, Vetrie D, Gorman P, Tomlinson IP, Carter NP.
    Genes Chromosomes Cancer; 2003 Apr 29; 36(4):361-74. PubMed ID: 12619160
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  • 14. Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH.
    Evers C, Beier M, Poelitz A, Hildebrandt B, Servan K, Drechsler M, Germing U, Royer HD, Royer-Pokora B.
    Genes Chromosomes Cancer; 2007 Dec 29; 46(12):1119-28. PubMed ID: 17823930
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  • 15. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE, Shim SH, Mark HF, Huang XL, Milunsky JM.
    Exp Mol Pathol; 2006 Jun 29; 80(3):262-6. PubMed ID: 16516886
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  • 16. Detection of copy number changes at the NF1 locus with improved high-resolution array CGH.
    Shen MH, Mantripragada K, Dumanski JP, Frayling I, Upadhyaya M.
    Clin Genet; 2007 Sep 29; 72(3):238-44. PubMed ID: 17718862
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  • 17. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
    Boehm D, Herold S, Kuechler A, Liehr T, Laccone F.
    Hum Mutat; 2004 Apr 29; 23(4):368-78. PubMed ID: 15024731
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  • 18. Microarray comparative genomic hybridization detection of chromosomal imbalances in uterine cervix carcinoma.
    Hidalgo A, Baudis M, Petersen I, Arreola H, Piña P, Vázquez-Ortiz G, Hernández D, González J, Lazos M, López R, Pérez C, García J, Vázquez K, Alatorre B, Salcedo M.
    BMC Cancer; 2005 Jul 09; 5():77. PubMed ID: 16004614
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