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Diabetic Medicine : a Journal of the British Diabetic Association|November 13, 2001
Analysis of the association between diabetic nephropathy and polymorphisms in the aldose reductase gene in Type 1 and Type 2 diabetes mellitusM Neamat-Allah, S A Feeney, D A Savage, et al.
Blood Cells, Molecules & Diseases|June 19, 2007
Pyruvate kinase deficient hemolytic anemia in the Northern Irish populationM J Percy, R van Wijk, S Haggan, et al.
Plos One|August 31, 2013
Telomere length and the risk of cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutationsLaura S Burke, Paula L Hyland, Ruth M Pfeiffer, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|January 27, 2020
Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic AnemiaLisa J McReynolds, Youjin Wang, Ashley S Thompson, et al.
AIDS (London, England)|July 24, 2019
Association between zidovudine-containing antiretroviral therapy exposure in utero and leukocyte telomere length at birthYoujin Wang, Sean S Brummel, Erin Beilstein-Wedel, et al.
Endocrine-Related Cancer|March 4, 2008
Parathyroid tumor development involves deregulation of homeobox genesH-C Jennifer Shen, Jennifer E Rosen, Lauren M Yang, et al.
British Journal of Cancer|October 29, 2011
Risk of renal cell carcinoma in relation to blood telomere length in a population-based case-control studyJ N Hofmann, A Baccarelli, K Schwartz, et al.
Human Mutation|September 2, 2017
Higher-than-expected population prevalence of potentially pathogenic germline TP53 variants in individuals unselected for cancer historyKelvin César de Andrade, Lisa Mirabello, Douglas R Stewart, et al.
Nature Genetics|May 16, 2006
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) regionDeborah J Smyth, Jason D Cooper, Rebecca Bailey, et al.
Human Molecular Genetics|September 1, 1997
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21N E Lamb, E Feingold, A Savage, et al.
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