id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_gvvyajofufglhls6u6yhxgyyge	Kathryn Beauregard	This Month in the Journal	2000.0	2	.pdf	application/pdf	1213	83	55	11p15.5 region, which is associated with Beckwith-Wiedemann syndrome and Wilms tumor, and the 15q11ABCR mutations lead to a clinically heterogeneous array of phenotypes, including Stargardt further evidence that sequence variation in ABCR is associated with age-related macular degeneration. TNNT1 Gene Mutation in Nemaline Myopathy, by Linkage Disequilibrium in the NF1 Gene Region, by a major impact on genetic-association studies, a greater recombination is associated with a change in the general APOE Haplotype Variation, by Fullerton et al. Individuals possessing an e4 allele have an increased risk of both diseases, whereas e2 is protective. More-complete examination of the alleles of APOE has to study further variation of APOE. population-specific distribution of APOE haplotypes. variation at the APOE locus. mutation that is present in the e2 and e3 alleles. Because LD measurements in different populations and different genetic regions have in genomewide association studies, and they will also Report (Mutational Hotspots in mtDNA), by Stoneking	./cache/work_gvvyajofufglhls6u6yhxgyyge.pdf	./txt/work_gvvyajofufglhls6u6yhxgyyge.txt