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Allelic imbalance analysis using a single-nucleotide polymorphism microarray for the detection of bladder cancer recurrence. [Journal Article]
Clin Cancer Res 2008 Dec 15; 14(24):8198-204.
Abstract | Full Citation | Find Related Articles | |
A global network for investigating the genomic epidemiology of malaria. [Journal Article, Research Support, Non-U.S. Gov't]
Nature 2008 Dec 11; 456(7223):732-7.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Pollin TI, Damcott CM, Shen H, et al.
A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Science 2008 Dec 12; 322(5908):1702-5.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Bergwitz C, Bastepe M
NHERF1 mutations and responsiveness of renal parathyroid hormone. [Comment, Letter]
N Engl J Med 2008 Dec 11; 359(24):2615-6; author reply 2616-7.
Full Citation | Find Related Articles | | Leibel RL
Energy in, energy out, and the effects of obesity-related genes. [Comment, Editorial]
N Engl J Med 2008 Dec 11; 359(24):2603-4.
Full Citation | Publisher Full Text | Find Related Articles | | Cecil JE, Tavendale R, Watt P, et al.
An obesity-associated FTO gene variant and increased energy intake in children. [Journal Article, Research Support, Non-U.S. Gov't]
N Engl J Med 2008 Dec 11; 359(24):2558-66.
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Shared and distinct genetic variants in type 1 diabetes and celiac disease. [Journal Article, Research Support, Non-U.S. Gov't]
N Engl J Med 2008 Dec 25; 359(26):2767-77.
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Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Am J Hum Genet 2008 Nov; 83(5):643-8.
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The genome-wide patterns of variation expose significant substructure in a founder population. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Am J Hum Genet 2008 Dec; 83(6):787-94.
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PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption. [Journal Article, Research Support, Non-U.S. Gov't]
Am J Hum Genet 2008 Dec; 83(6):781-6.
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