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Correlation of Polyp Number and Family History of Colon Cancer With Germline MYH Mutations
Won–Seok Jo, Prathap Bandipalliam, Kristen M. Shannon, Kristin B. Niendorf, Gayun Chan–Smutko, Chin Hur, Sapna Syngal, Daniel C. Chung Clinical Gastroenterology and Hepatology Volume 3, Issue 10, Pages (October 2005) DOI: /S (05) Copyright © 2005 American Gastroenterological Association Terms and Conditions
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Figure 1 Gel electrophoresis of exon 13 polymerase chain reaction products from selected patients after digestion with Bgl II restriction enzyme. The G382D mutation introduces a Bgl II restriction site not present in the wild-type sequence. Patient 214 has a G382D mutation. Clinical Gastroenterology and Hepatology 2005 3, DOI: ( /S (05) ) Copyright © 2005 American Gastroenterological Association Terms and Conditions
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Figure 2 DNA sequence chromatogram showing a Y165C homozygous mutation in patient 642. There is 1 peak corresponding to the presence of an adenine to guanine missense substitution in both alleles. Clinical Gastroenterology and Hepatology 2005 3, DOI: ( /S (05) ) Copyright © 2005 American Gastroenterological Association Terms and Conditions
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Figure 3 DNA sequence chromatogram showing a G382D heterozygous mutation in patient 273. In codon 382 there are 2 peaks corresponding to an adenine missense mutation in 1 allele and to a wild-type guanine in the second allele. Clinical Gastroenterology and Hepatology 2005 3, DOI: ( /S (05) ) Copyright © 2005 American Gastroenterological Association Terms and Conditions
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