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It's really not that hard to use each word in its proper manner.
’s
Thi's user know's that not every word that end's with s need's an apostrophe and will remove misused apostrophe's from Wikipedia with extreme prejudice.
. The
This user does not put two spaces after a full stop.
^Wintle RF, Nygaard TG, Herbrick JS, et al. (1997). Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q. Genomics 40:409-414
^Wintle RF, Costa T, Haslam RHA, et al. (1995). Molecular analysis redefines three human chromosome 14 deletions. Hum. Genet. 95:495-500
^Wintle RF and Cox DW (1994). Mapping of human immunoglobulin heavy chain variable gene segments outside the major IGH locus. Genomics 23:151-157
^Sanyal S, Wintle RF (co-first authors), Kindt KS, et al. (2004). Dopamine modulates the plasticity of mechanosensory responses in C. elegans. EMBO J. 23(2):473-82
^Wintle RF and Van Tol HHM (2001). Dopamine signaling in C. elegans – potential for parkinsonism research. Parkinsonism Rel. Disord. 7(3):177-183
^Newman WG, Gu X, Wintle R.F., et al. (2006). DLG5 variants contribute to Crohn disease risk in a Canadian population. Hum. Mutat. 27(4):353-358
^Newman B, Gu X, Wintle R, et al. (2005). A risk haplotype in the SLC22A4/SLC22A5 gene cluster influences phenotypic expression of Crohn’s Disease. Gastroenterology 128(2):260-9
^Peltekova VD, Wintle RF, Rubin LA, et al. (2004). Functional variants of OCTN transporter genes are associated with Crohn’s Disease. Nature Genet. 36(5):471-75
^Newman B, Wintle RF, Van Oene M., et al. (2005). SLC22A4 polymorphisms implicated in Rheumatoid Arthritis and Crohn’s Disease are not associated with Rheumatoid Arthritis in a Canadian caucasian population. Arthritis Rheum. 52(2):425-9
^Feuk L, Marshall CR, Wintle RF, et al. (2006). Structural variants: changing the landscape of chromosomes and design of disease studies. Hum. Mol. Genet. 15:R57-R66
^Goobie S, Knijnenburg J, FitzPatrick D, et al. (2008). Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting. Cytogenet. Genome Res. 123:65-78
^Uddin M, Thiruvahindrapuram B, Walker S, et al. (2014). A high-resolution copy-number variation resource for clinical and population genetics.Genet Med 2014 Dec 11. doi: 10.1038/gim.2014.178
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