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Clinical phenotype associated with terminal 2q37 deletion.
Conrad B, Dewald G, Christensen E, Lopez M, Higgins J, Pierpont ME. Conrad B, et al. Clin Genet. 1995 Sep;48(3):134-9. doi: 10.1111/j.1399-0004.1995.tb04073.x. Clin Genet. 1995. PMID: 8556820 Review.
Analysis of the RNASEL gene in familial and sporadic prostate cancer.
Wang L, McDonnell SK, Elkins DA, Slager SL, Christensen E, Marks AF, Cunningham JM, Peterson BJ, Jacobsen SJ, Cerhan JR, Blute ML, Schaid DJ, Thibodeau SN. Wang L, et al. Am J Hum Genet. 2002 Jul;71(1):116-23. doi: 10.1086/341281. Epub 2002 May 17. Am J Hum Genet. 2002. PMID: 12022038 Free PMC article.
The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.
Cunningham JM, Kim CY, Christensen ER, Tester DJ, Parc Y, Burgart LJ, Halling KC, McDonnell SK, Schaid DJ, Walsh Vockley C, Kubly V, Nelson H, Michels VV, Thibodeau SN. Cunningham JM, et al. Among authors: christensen er. Am J Hum Genet. 2001 Oct;69(4):780-90. doi: 10.1086/323658. Epub 2001 Aug 24. Am J Hum Genet. 2001. PMID: 11524701 Free PMC article.
70 results