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Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome

2002; Wiley; Volume: 19; Issue: 4 Linguagem: Inglês

10.1002/humu.10088

1098-1004

Richard G.H. Cotton,

Genomics and Phylogenetic Studies

Human MutationVolume 19, Issue 4 p. 313-314 EditorialFree Access Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome Richard G.H. Cotton, Richard G.H. Cotton Genomic Disorders Research Centre, St. Vincent's Hospital Melbourne, Fitzroy, Australia The University of Melbourne, Department of Medicine, Melbourne, AustraliaSearch for more papers by this author Richard G.H. Cotton, Richard G.H. Cotton Genomic Disorders Research Centre, St. Vincent's Hospital Melbourne, Fitzroy, Australia The University of Melbourne, Department of Medicine, Melbourne, AustraliaSearch for more papers by this author First published: 18 March 2002 https://doi.org/10.1002/humu.10088Citations: 17AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. REFERENCES Amos J, Patnaik M. 2002. Commercial molecular diagnostics in the U.S.: the human genome project to the clinical laboratory. Hum Mutat 19: 324– 333. Cotton RGH, Glavač D. 2001. Mutation detection 2001: sixth international symposium on mutations in the human genome, May 3–7, Bled, Slovenia. Hum Mutat 18: 542– 544. Czeizel A, Sankaranarayanan K. 1984. The load of genetic and partially genetic disorders in man. Mutat Res 128: 73– 103. Ganguly A. 2002. An update on conformation sensitive gel electrophoresis. Hum Mutat 19: 334– 342. Glavač D, Potočnik U, Podpečnik D, Žižek T, Smerkolj S, Ravnik-Glavač M. 2002. Correlation of MFOLD-predicted DNA secondary structures with separation patterns obtained by capillary electrophores is single-strand conformation polymorphism (CE-SSCP) analysis. Hum Mutat 19: 384– 394. Kolchinsky A, Mirzabekov A. 2002. Analysis of SNPs and other genomic variations using gel-based chips. Hum Mutat 19: 343– 360. Kwok P. 2002. SNP genotyping with fluorescence polarization detection. Hum Mutat 19: 315– 323. Lu M, Shortreed M, Hall J, Wang L, Berggren T, Wilkins Stevens P, Kelso D, Lyamichev V, Neri B, Smith L. 2002. A surface invasive cleavage assay for highly parallel SNP analysis. Hum Mutat 19: 416– 422. Nilsson M, Banér J, Mendel-Hartvig M, Dahl F, Antson D, Gullberg M, Landegren U. 2002. Making ends meet in genetic analysis using padlock probes. Hum Mutat 19: 410– 415. Nordfors L, Jansson M, Sandberg G, Lavebratt C, Sengul S, Schalling M, Arner P. 2002. Large-scale genotyping of single nucleotide polymorphisms by Pyrosequencing™ and validation against the 5′ nuclease (TaqMan®) assay. Hum Mutat 19: 395– 401. Perlin M, Szabady B. 2002. Determining sequence length or content in zero, one, and two dimensions. Hum Mutat 19: 361– 373. Ravnik-Glavač M, Atkinson A, Glavač D, Dean M. 2002. DHPLC screening of cystic fibrosis gene mutations. Hum Mutat 19: 374– 383. Warrington A, Shah N, Chen X, Janis M, Liu C, Kondapalli S, Reyes V, Savage M, Zhang Z, Watts R, DeGuzman M, Berno A, Snyder J, Baid J. 2002. New developments in high throughput resequencing and variation detection using high density microarrays. Hum Mutat 19: 402– 409. Citing Literature Volume19, Issue4April 2002Pages 313-314 ReferencesRelatedInformation