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Polymorphism, Single Nucleotide journal articles from PubMed MEDLINE database

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Tefferi A, Vardiman JW 
Myelodysplastic syndromes. [Journal Article, Review]
N Engl J Med 2009 Nov 5; 361(19):1872-85.
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Friedman SH 
Postpartum mood disorders: genetic progress and treatment paradigms. [Comment, Comparative Study, Editorial]
Am J Psychiatry 2009 Nov; 166(11):1201-4.
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Jones GT, van Rij AM 
Regarding "Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association". [Comment, Letter]
J Vasc Surg 2009 Nov; 50(5):1246-7; author reply 1247.
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Sevransky J 
Is it time for intensivists to learn genomics? [Comment, Editorial]
Crit Care Med 2009 Oct; 37(10):2852-3.
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Gehmert S, Velapatiño B, Herrera P, et al. 
Interleukin-1 beta single-nucleotide polymorphism's C allele is associated with elevated risk of gastric cancer in Helicobacter pylori-infected Peruvians. [Journal Article, Research Support, N.I.H., Extramural]
Am J Trop Med Hyg 2009 Nov; 81(5):804-10.
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Azria D, Ozsahin M, Rosenstein B 
Radiation-Induced Sequelae Measured by Means of Lymphocyte Apoptosis: Importance of Certain Single Nucleotide Polymorphisms: In Regard to Schnarr et al. (Int J Radiat Oncol Biol Phys 2009). [LETTER]
Int J Radiat Oncol Biol Phys 2009 Nov 15; 75(4):1275.
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Chu AY, Parekh RS, Astor BC, et al. 
Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study. [JOURNAL ARTICLE]
BMC Med Genet 2009 Oct 23; 10(1):108.
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Taioli E, Garza MA, Ahn YO, et al. 
Meta- and pooled analyses of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and colorectal cancer: a HuGE-GSEC review. [Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S.]
Am J Epidemiol 2009 Nov 15; 170(10):1207-21.
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Reding KW, Li CI, Weiss NS, et al. 
Genetic variation in the progesterone receptor and metabolism pathways and hormone therapy in relation to breast cancer risk. [Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.]
Am J Epidemiol 2009 Nov 15; 170(10):1241-9.
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Hartmaier RJ, Walenkamp MJ, Richter AS, et al. 
A case of premature thelarche with no central cause or genetic variants within the estrogen receptor signaling pathway. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.]
J Pediatr Endocrinol Metab 2009 Aug; 22(8):751-8.
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