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Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium.
Aronson M, Gallinger S, Cohen Z, Cohen S, Dvir R, Elhasid R, Baris HN, Kariv R, Druker H, Chan H, Ling SC, Kortan P, Holter S, Semotiuk K, Malkin D, Farah R, Sayad A, Heald B, Kalady MF, Penney LS, Rideout AL, Rashid M, Hasadsri L, Pichurin P, Riegert-Johnson D, Campbell B, Bakry D, Al-Rimawi H, Alharbi QK, Alharbi M, Shamvil A, Tabori U, Durno C. Aronson M, et al. Am J Gastroenterol. 2016 Feb;111(2):275-84. doi: 10.1038/ajg.2015.392. Epub 2016 Jan 5. Am J Gastroenterol. 2016. PMID: 26729549
Heterozygosity for the BLM(Ash) mutation and cancer risk.
Cleary SP, Zhang W, Di Nicola N, Aronson M, Aube J, Steinman A, Haddad R, Redston M, Gallinger S, Narod SA, Gryfe R. Cleary SP, et al. Among authors: aronson m. Cancer Res. 2003 Apr 15;63(8):1769-71. Cancer Res. 2003. PMID: 12702560
Hereditary nonpolyposis colorectal cancer--molecular basis.
Brezden-Masley C, Aronson MD, Bapat B, Pollett A, Gryfe R, Redston M, Gallinger S. Brezden-Masley C, et al. Among authors: aronson md. Surgery. 2003 Jul;134(1):29-33. doi: 10.1067/msy.2003.176. Surgery. 2003. PMID: 12874579 Review. No abstract available.
Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation.
Gallinger S, Aronson M, Shayan K, Ratcliffe EM, Gerstle JT, Parkin PC, Rothenmund H, Croitoru M, Baumann E, Durie PR, Weksberg R, Pollett A, Riddell RH, Ngan BY, Cutz E, Lagarde AE, Chan HS. Gallinger S, et al. Among authors: aronson m. Gastroenterology. 2004 Feb;126(2):576-85. doi: 10.1053/j.gastro.2003.11.008. Gastroenterology. 2004. PMID: 14762794
568 results