DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2-Reference-Cited by-同舟云学术

DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2

Published:2001-01 Issue:1-2 Volume:47 Page:21-32
ISSN:0165-022X
Container-title:Journal of Biochemical and Biophysical Methods
language:en
Short-container-title:Journal of Biochemical and Biophysical Methods

Author:

Holinski-Feder Elke,Müller-Koch Y,Friedl W,Moeslein G,Keller G,Plaschke J,Ballhausen W,Gross M,Baldwin-Jedele K,Jungck M,Mangold E,Vogelsang H,Schackert H.-K,Lohsea P,Murken J,Meitinger Th

Publisher

Elsevier BV

Subject

Biochemistry,Biophysics

Reference9 articles.

1. DNA mutation detection using denaturing high-performance liquid chromatography;Oefner,1998

2. Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography;Underhill;Genome Res,1997

3. Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection;O’Donovan;Genomics,1998

4. Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders;Liu;Genet Test,1997

5. Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations;Wagner;Genomics,1999

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