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158 related items for PubMed ID: 16541397
1. Determination of genomic copy number with quantitative microsphere hybridization. Newkirk HL, Rogan PK, Miralles M, Knoll JH. Hum Mutat; 2006 Apr; 27(4):376-86. PubMed ID: 16541397 [Abstract] [Full Text] [Related]
2. High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probes. Reid AG, Tarpey PS, Nacheva EP. Genes Chromosomes Cancer; 2003 Jul; 37(3):282-90. PubMed ID: 12759926 [Abstract] [Full Text] [Related]
3. Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array. Newkirk HL, Bittel DC, Butler MG. Am J Med Genet A; 2008 Sep 15; 146A(18):2346-54. PubMed ID: 18698613 [Abstract] [Full Text] [Related]
4. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D, Collins C, Kuo WL, Chen C, Zhai Y, Dairkee SH, Ljung BM, Gray JW, Albertson DG. Nat Genet; 1998 Oct 15; 20(2):207-11. PubMed ID: 9771718 [Abstract] [Full Text] [Related]
5. A new quantitative PCR multiplex assay for rapid analysis of chromosome 17p11.2-12 duplications and deletions leading to HMSN/HNPP. Thiel CT, Kraus C, Rauch A, Ekici AB, Rautenstrauss B, Reis A. Eur J Hum Genet; 2003 Feb 15; 11(2):170-8. PubMed ID: 12634865 [Abstract] [Full Text] [Related]
6. A method for accurate detection of genomic microdeletions using real-time quantitative PCR. Weksberg R, Hughes S, Moldovan L, Bassett AS, Chow EW, Squire JA. BMC Genomics; 2005 Dec 13; 6():180. PubMed ID: 16351727 [Abstract] [Full Text] [Related]
7. Multiplex quantitative competitive polymerase chain reaction based on a multianalyte hybridization assay performed on spectrally encoded microspheres. Kalogianni DP, Elenis DS, Christopoulos TK, Ioannou PC. Anal Chem; 2007 Sep 01; 79(17):6655-61. PubMed ID: 17645311 [Abstract] [Full Text] [Related]
8. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer. Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES. BMC Genomics; 2007 Feb 20; 8():53. PubMed ID: 17311676 [Abstract] [Full Text] [Related]
9. Diagnosis of haploidy and triploidy based on measurement of gene copy number by real-time PCR. Wilke K, Duman B, Horst J. Hum Mutat; 2000 Nov 20; 16(5):431-6. PubMed ID: 11058901 [Abstract] [Full Text] [Related]
10. Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes. Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A, Patsalis PC. Nat Protoc; 2008 Nov 20; 3(5):849-65. PubMed ID: 18451793 [Abstract] [Full Text] [Related]
11. Improved testing for CMT1A and HNPP using multiplex ligation-dependent probe amplification (MLPA) with rapid DNA preparations: comparison with the interphase FISH method. Slater H, Bruno D, Ren H, La P, Burgess T, Hills L, Nouri S, Schouten J, Choo KH. Hum Mutat; 2004 Aug 20; 24(2):164-71. PubMed ID: 15241798 [Abstract] [Full Text] [Related]
12. Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization. Patsalis PC, Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A. Eur J Hum Genet; 2007 Feb 20; 15(2):162-72. PubMed ID: 17119536 [Abstract] [Full Text] [Related]
13. Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia. Braude I, Vukovic B, Prasad M, Marrano P, Turley S, Barber D, Zielenska M, Squire JA. BMC Genomics; 2006 Jun 06; 7():138. PubMed ID: 16756668 [Abstract] [Full Text] [Related]
14. [A novel oligonucleotide arrays-based multiplex amplifiable probe hybridization technology]. Liu HP, Wang H, Lu ZH, Liu XP, Xia K, Xia JH. Yi Chuan Xue Bao; 2004 Feb 06; 31(2):119-24. PubMed ID: 15473300 [Abstract] [Full Text] [Related]
15. Comparative genomic hybridization for analysis of changes in DNA copy number in multiple myeloma. Rao PH. Methods Mol Med; 2005 Feb 06; 113():71-83. PubMed ID: 15968096 [Abstract] [Full Text] [Related]
16. Integrative genomic analysis of small-cell lung carcinoma reveals correlates of sensitivity to bcl-2 antagonists and uncovers novel chromosomal gains. Olejniczak ET, Van Sant C, Anderson MG, Wang G, Tahir SK, Sauter G, Lesniewski R, Semizarov D. Mol Cancer Res; 2007 Apr 06; 5(4):331-9. PubMed ID: 17426248 [Abstract] [Full Text] [Related]
17. Microarray MAPH: accurate array-based detection of relative copy number in genomic DNA. Gibbons B, Datta P, Wu Y, Chan A, Al Armour J. BMC Genomics; 2006 Jun 30; 7():163. PubMed ID: 16813644 [Abstract] [Full Text] [Related]
18. Across array comparative genomic hybridization: a strategy to reduce reference channel hybridizations. Buffart TE, Israeli D, Tijssen M, Vosse SJ, Mrsić A, Meijer GA, Ylstra B. Genes Chromosomes Cancer; 2008 Nov 30; 47(11):994-1004. PubMed ID: 18663753 [Abstract] [Full Text] [Related]
19. Gene expression profiling and gene copy-number changes in malignant mesothelioma cell lines. Zanazzi C, Hersmus R, Veltman IM, Gillis AJ, van Drunen E, Beverloo HB, Hegmans JP, Verweij M, Lambrecht BN, Oosterhuis JW, Looijenga LH. Genes Chromosomes Cancer; 2007 Oct 30; 46(10):895-908. PubMed ID: 17620293 [Abstract] [Full Text] [Related]
20. Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison. Hung CC, Lee CN, Lin CY, Cheng WF, Chen CA, Hsieh ST, Yang CC, Jong YJ, Su YN, Lin WL. Electrophoresis; 2008 Feb 30; 29(3):618-25. PubMed ID: 18200636 [Abstract] [Full Text] [Related] Page: [Next] [New Search]