Copyright
©The Author(s) 2005.
World J Gastroenterol. Oct 7, 2005; 11(37): 5770-5776
Published online Oct 7, 2005. doi: 10.3748/wjg.v11.i37.5770
Published online Oct 7, 2005. doi: 10.3748/wjg.v11.i37.5770
Figure 1 Pedigrees and DNA nucleotide sequence of the three families with disease-causing mutations of hMSH6 gene.
Squares, males; circles, females; diagonal bars, deceased; unblackened symbols, no tumor; semi-blackened symbols, patients with histological-verified carcinomas; arrows, probands; mut, carries the indicated mutation. Abbreviations indicating type of tumor: CRC, colorectal; SI, small intestine; G, gastric; H, Hodgkin; End, endometrium; Pr, prostate; L, liver. Number after abbreviation indicates age at which tumor was diagnosed. Electropherograms of the wild type and mutant nucleotide sequences for V878A and Q263X mutations located in exon 4 of the hMSH6 gene.
- Citation: Abajo AS, Hoya ML, Tosar A, Godino J, Fernández JM, Asenjo JL, Villamil BP, Segura PP, Diaz-Rubio E, Caldes T. Low prevalence of germline hMSH6 mutations in colorectal cancer families from Spain. World J Gastroenterol 2005; 11(37): 5770-5776
- URL: https://www.wjgnet.com/1007-9327/full/v11/i37/5770.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i37.5770