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Showing results 354 to 366 of 366 < previous 
PreviewIssue DateTitleAuthor(s)
2009Variation in Giardia: towards a taxonomic revision of the genusMonis, P.; Caccio, S.; Thompson, R.
1998A very high density microsatellite map (1 STR/41kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical regionCox, Timothy C.; Cox, Liza L.; Ballabio, Andrea
2015Vulnerability to climate change adaptation in rural BangladeshShaw, Jennie
2014Whole exome sequencing of extreme morbid obesity patients: translational implications for obesity and related disordersPaz-Filho, G.; Boguszewski, M.; Mastronardi, C.; Patel, H.; Johar, A.; Chuah, A.; Huttley, G.; Boguszewski, C.; Wong, M.; Arcos-Burgos, M.; Licinio, J.
2016Whole genome comparison reveals high levels of inbreeding and strain redundancy across the spectrum of commercial wine strains of Saccharomyces cerevisiaeBorneman, A.; Forgan, A.; Kolouchova, R.; Fraser, J.; Schmidt, S.
2015Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populationsPengelly, R.; Tapper, W.; Gibson, J.; Knut, M.; Tearle, R.; Collins, A.; Ennis, S.
2015WWOX, the chromosomal fragile site FRA16D spanning gene: its role in metabolism and contribution to cancerRichards, R.; Choo, A.; Lee, C.; Dayan, S.; O Keefe, L.
1995X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndromeGedeon, A.; Wilson, M.; Colley, A.; Sillence, D.; Mulley, J.
1995X-Y chromosome dissociation in mice and rats exposed to increased testicular or environmental temperaturesVan Zelst, S.; Zupp, J.; Hayman, D.; Setchell, B.
2013Y-Chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populationsBadro, D.; Douaihy, B.; Haber, M.; Youhanna, S.; Salloum, A.; Ghassibe-Sabbagh, M.; Johnsrud, B.; Khazen, G.; Matisoo-Smith, E.; Soria-Hernanz, D.; Wells, R.; Tyler-Smith, C.; Platt, D.; Zalloua, P.
2017YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunctionGabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al.
2009Zebrafish aplnra functions in epibolyNornes, S.; Tucker, B.; Lardelli, M.
2018The zebrafish orthologue of familial Alzheimer's disease gene PRESENILIN 2 is required for normal adult melanotic skin pigmentationJiang, H.; Newman, M.; Lardelli, M.