Kohonen-Corish M - Search Results

1

Molecular characterization of patients with 18q23 deletions.

Strathdee G, Sutherland R, Jonsson JJ, Sataloff R, Kohonen-Corish M, Grady D, Overhauser J. Strathdee G, et al. Am J Hum Genet. 1997 Apr;60(4):860-8. Am J Hum Genet. 1997. PMID: 9106532 Free PMC article.

2

A new deletion of 18q23 with few typical features of the 18q- syndrome.

Kohonen-Corish M, Strathdee G, Overhauser J, McDonald T, Jammu V. Kohonen-Corish M, et al. J Med Genet. 1996 Mar;33(3):240-3. doi: 10.1136/jmg.33.3.240. J Med Genet. 1996. PMID: 8728701 Free PMC article.

3

A highly polymorphic CA/GT repeat in intron 3 of the human urokinase receptor gene (PLAUR).

Kohonen-Corish MR, Wang Y, Doe WF. Kohonen-Corish MR, et al. Hum Genet. 1996 Jan;97(1):124-5. doi: 10.1007/BF00218847. Hum Genet. 1996. PMID: 8557253

4

Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16.

Cavanaugh JA, Callen DF, Wilson SR, Stanford PM, Sraml ME, Gorska M, Crawford J, Whitmore SA, Shlegel C, Foote S, Kohonen-Corish M, Pavli P. Cavanaugh JA, et al. Ann Hum Genet. 1998 Jul;62(Pt 4):291-8. doi: 10.1046/j.1469-1809.1998.6240291.x. Ann Hum Genet. 1998. PMID: 9924607

5

Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?

Kariola R, Otway R, Lönnqvist KE, Raevaara TE, Macrae F, Vos YJ, Kohonen-Corish M, Hofstra RM, Nyström-Lahti M. Kariola R, et al. Hum Genet. 2003 Feb;112(2):105-9. doi: 10.1007/s00439-002-0866-4. Epub 2002 Nov 21. Hum Genet. 2003. PMID: 12522549

6

Chromosome 2p linkage analysis in hereditary non-polyposis colon cancer.

Kohonen-Corish MR, Doe WF, St John DJ, Macrae FA. Kohonen-Corish MR, et al. J Gastroenterol Hepatol. 1995 Jan-Feb;10(1):76-80. doi: 10.1111/j.1440-1746.1995.tb01052.x. J Gastroenterol Hepatol. 1995. PMID: 7620112

7

A polymorphic marker for the human cathepsin B gene.

MacKenzie JR, Mason SL, Hickford JG, Kohonen-Corish MR, Bickerstaffe R. MacKenzie JR, et al. Mol Cell Probes. 2001 Aug;15(4):235-7. doi: 10.1006/mcpr.2001.0362. Mol Cell Probes. 2001. PMID: 11513559

8

Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.

Otway R, Tetlow N, Hornby J, Doe WF, Kohonen-Corish MR. Otway R, et al. Hum Genet. 2005 May;116(6):536. Hum Genet. 2005. PMID: 15991308 No abstract available.

9

Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.

Otway R, Tetlow N, Hornby J, Doe WF, Kohonen-Corish MR. Otway R, et al. Hum Genet. 2005 May;116(6):536. Hum Genet. 2005. PMID: 15991307 No abstract available.

10

Gene symbol: MLH1. Disease: Hereditary nonpolyposis colorectal cancer.

Otway R, Tetlow N, Hornby J, Doe WF, Kohonen-Corish MR. Otway R, et al. Hum Genet. 2005 May;116(6):535. Hum Genet. 2005. PMID: 15991306 No abstract available.

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