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Showing results 435 to 446 of 446 < previous

Preview	Issue Date	Title	Author(s)
	2009	Variation in Giardia: towards a taxonomic revision of the genus	Monis, P.; Caccio, S.; Thompson, R.
	1998	A very high density microsatellite map (1 STR/41kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical region	Cox, Timothy C.; Cox, Liza L.; Ballabio, Andrea
	2015	Vulnerability to climate change adaptation in rural Bangladesh	Shaw, Jennie,; Grubb, Michael,
	2014	Whole exome sequencing of extreme morbid obesity patients: translational implications for obesity and related disorders	Paz-Filho, G.; Boguszewski, M.; Mastronardi, C.; Patel, H.; Johar, A.; Chuah, A.; Huttley, G.; Boguszewski, C.; Wong, M.; Arcos-Burgos, M.; Licinio, J.
	2016	Whole genome comparison reveals high levels of inbreeding and strain redundancy across the spectrum of commercial wine strains of Saccharomyces cerevisiae	Borneman, A.; Forgan, A.; Kolouchova, R.; Fraser, J.; Schmidt, S.
	2015	Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations	Pengelly, R.; Tapper, W.; Gibson, J.; Knut, M.; Tearle, R.; Collins, A.; Ennis, S.
	2015	WWOX, the chromosomal fragile site FRA16D spanning gene: its role in metabolism and contribution to cancer	Richards, R.I.; Choo, A.; Lee, C.S.; Dayan, S.; O Keefe, L.
	1995	X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome	Gedeon, A.; Wilson, M.; Colley, A.; Sillence, D.; Mulley, J.
	1995	X-Y chromosome dissociation in mice and rats exposed to increased testicular or environmental temperatures	Van Zelst, S.; Zupp, J.; Hayman, D.; Setchell, B.
	2013	Y-Chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populations	Badro, 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.; Caramelli, D.
	2017	YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction	Gabriele, 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.
	2009	Zebrafish aplnra functions in epiboly	Nornes, S.; Tucker, B.; Lardelli, M.

Showing results 435 to 446 of 446 < previous