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	61.	A genetic linkage map with 29 loci spanning human chromosome 13q. [electronic resource] by Gerken, S Leppert, M O'Connell, P Cavenee, W James, C D Ballard, L Stauffer, D Elsner, T Plaetke, R Lalouel, J M Producer: 19930726 In: Genomics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22. [electronic resource] by Hoehe, M R Plaetke, R Otterud, B Stauffer, D Holik, J Byerley, W F Baetge, E E Gershon, E S Lalouel, J M Leppert, M Producer: 19930623 In: Human molecular genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Apolipoprotein polymorphisms fail to define risk of coronary artery disease. Results of a prospective, angiographically controlled study. [electronic resource] by Marshall, H W Morrison, L C Wu, L L Anderson, J L Corneli, P S Stauffer, D M Allen, A Karagounis, L A Ward, R H Producer: 19940318 In: Circulation vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Genetic mapping of adrenergic receptor genes in humans. [electronic resource] by Hoehe, M R Otterud, B Hsieh, W T Martinez, M M Stauffer, D Holik, J Berrettini, W H Byerley, W F Gershon, E S Lalouel, J M Producer: 19951212 In: Journal of molecular medicine (Berlin, Germany) vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	C-terminal interaction is essential for surface trafficking but not for heteromeric assembly of GABA(b) receptors. [electronic resource] by Pagano, A Rovelli, G Mosbacher, J Lohmann, T Duthey, B Stauffer, D Ristig, D Schuler, V Meigel, I Lampert, C Stein, T Prezeau, L Blahos, J Pin, J Froestl, W Kuhn, R Heid, J Kaupmann, K Bettler, B Producer: 20010607 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	66.	A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. [electronic resource] by Singh, N A Charlier, C Stauffer, D DuPont, B R Leach, R J Melis, R Ronen, G M Bjerre, I Quattlebaum, T Murphy, J V McHarg, M L Gagnon, D Rosales, T O Peiffer, A Anderson, V E Leppert, M Producer: 19980129 In: Nature genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. [electronic resource] by Allikmets, R Singh, N Sun, H Shroyer, N F Hutchinson, A Chidambaram, A Gerrard, B Baird, L Stauffer, D Peiffer, A Rattner, A Smallwood, P Li, Y Anderson, K L Lewis, R A Nathans, J Leppert, M Dean, M Lupski, J R Producer: 19970404 In: Nature genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)