McPhillips ML - Search Results

1

cDNA analysis of the BRCA1 unclassified variant c.5194-12G>A.

Wong-Brown MW, McPhillips ML, Hipwell M, Pecenpetelovska G, Dooley S, Meldrum C, Scott RJ. Wong-Brown MW, et al. Among authors: mcphillips ml. Clin Genet. 2013 Nov;84(5):505-6. doi: 10.1111/cge.12052. Epub 2012 Dec 20. Clin Genet. 2013. PMID: 23278966 No abstract available.

2

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds.

Scott RJ, McPhillips M, Meldrum CJ, Fitzgerald PE, Adams K, Spigelman AD, du Sart D, Tucker K, Kirk J. Scott RJ, et al. Am J Hum Genet. 2001 Jan;68(1):118-127. doi: 10.1086/316942. Epub 2000 Dec 7. Am J Hum Genet. 2001. PMID: 11112663 Free PMC article.

3

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.

Scott RJ, Crooks R, Meldrum CJ, Thomas L, Smith CJ, Mowat D, McPhillips M, Spigelman AD. Scott RJ, et al. Clin Genet. 2002 Oct;62(4):282-7. doi: 10.1034/j.1399-0004.2002.620405.x. Clin Genet. 2002. PMID: 12372054

4

Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations.

Thompson E, Meldrum CJ, Crooks R, McPhillips M, Thomas L, Spigelman AD, Scott RJ. Thompson E, et al. Clin Genet. 2004 Mar;65(3):215-25. doi: 10.1111/j.1399-0004.2004.00214.x. Clin Genet. 2004. PMID: 14756672

5

The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria.

Ashton KA, Meldrum CJ, McPhillips ML, Suchy J, Kurzawski G, Lubinski J, Scott RJ. Ashton KA, et al. Among authors: mcphillips ml. Hered Cancer Clin Pract. 2006 May 15;4(2):94-102. doi: 10.1186/1897-4287-4-2-94. Hered Cancer Clin Pract. 2006. PMID: 20223014 Free PMC article.

6

Deletion Mutations in an Australian Series of HNPCC Patients.

McPhillips M, Meldrum CJ, Creegan R, Edkins E, Scott RJ. McPhillips M, et al. Hered Cancer Clin Pract. 2005 Nov 15;3(1):43-7. doi: 10.1186/1897-4287-3-1-43. Hered Cancer Clin Pract. 2005. PMID: 20223028 Free PMC article.

7

Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients.

Ashton KA, Meldrum CJ, McPhillips ML, Kairupan CF, Scott RJ. Ashton KA, et al. Among authors: mcphillips ml. Hered Cancer Clin Pract. 2005 May 15;3(2):65-70. doi: 10.1186/1897-4287-3-2-65. Hered Cancer Clin Pract. 2005. PMID: 20223032 Free PMC article.

8

MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.

Talseth-Palmer BA, McPhillips M, Groombridge C, Spigelman A, Scott RJ. Talseth-Palmer BA, et al. Hered Cancer Clin Pract. 2010 May 21;8(1):5. doi: 10.1186/1897-4287-8-5. Hered Cancer Clin Pract. 2010. PMID: 20487569 Free PMC article.

9

Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome.

Talseth-Palmer BA, Brenne IS, Ashton KA, Evans TJ, McPhillips M, Groombridge C, Suchy J, Kurzawski G, Spigelman A, Lubinski J, Scott RJ. Talseth-Palmer BA, et al. J Med Genet. 2011 Apr;48(4):279-84. doi: 10.1136/jmg.2010.079962. Epub 2010 Nov 19. J Med Genet. 2011. PMID: 21097774

10

Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.

Talseth-Palmer BA, Wijnen JT, Brenne IS, Jagmohan-Changur S, Barker D, Ashton KA, Tops CM, Evans TJ, McPhillips M, Groombridge C, Suchy J, Kurzawski G; Dutch Cancer Genetics Group; Spigelman A, Møller P, Morreau HM, Van Wezel T, Lubinski J, Vasen HF, Scott RJ. Talseth-Palmer BA, et al. Int J Cancer. 2013 Apr 1;132(7):1556-64. doi: 10.1002/ijc.27843. Epub 2012 Oct 11. Int J Cancer. 2013. PMID: 22987364 Free article.

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