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	121.	Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. [electronic resource] by Foroud, T Uniacke, S K Liu, L Pankratz, N Rudolph, A Halter, C Shults, C Marder, K Conneally, P M Nichols, W C Producer: 20040209 In: Neurology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. [electronic resource] by Dlouhy, S R Hsiao, K Farlow, M R Foroud, T Conneally, P M Johnson, P Prusiner, S B Hodes, M E Ghetti, B Producer: 19930610 In: Nature genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	A genetic linkage map of the long arm of human chromosome 22. [electronic resource] by Rouleau, G A Haines, J L Bazanowski, A Colella-Crowley, A Trofatter, J A Wexler, N S Conneally, P M Gusella, J F Producer: 19890323 In: Genomics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	Motor changes in presymptomatic Huntington disease gene carriers. [electronic resource] by Siemers, E Foroud, T Bill, D J Sorbel, J Norton, J A Hodes, M E Niebler, G Conneally, P M Christian, J C Producer: 19960726 In: Archives of neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. [electronic resource] by Rivas, M L Conneally, P M Hecht, F Lovrien, E W Magenis, E Merritt, A D Meyers, D A Palmer, C G Wang, L Producer: 19760220 In: Cytogenetics and cell genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. [electronic resource] by Rivas, M L Conneally, P M Hecht, F Lovrien, E W Magenis, E Merritt, A D Meyers, D A Palmer, C G Wang, L Producer: 19760324 In: Birth defects original article series vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	127.	Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family. [electronic resource] by Ghetti, B Tagliavini, F Masters, C L Beyreuther, K Giaccone, G Verga, L Farlow, M R Conneally, P M Dlouhy, S R Azzarelli, B Producer: 19891218 In: Neurology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	Linkage relations of the loci for the MN blood group and red cell acid phosphatase. [electronic resource] by Weitkamp, L R Lovrien, E W Olaisen, B Fenger, K Gedde-Dahl, T Sorensen, S A Conneally, P M Bias, W B Ott, J Producer: 19760220 In: Cytogenetics and cell genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19. [electronic resource] by Koller, D L White, K E Liu, G Hui, S L Conneally, P M Johnston, C C Econs, M J Foroud, T Peacock, M Producer: 20040211 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. [electronic resource] by Hsiao, K Dlouhy, S R Farlow, M R Cass, C Da Costa, M Conneally, P M Hodes, M E Ghetti, B Prusiner, S B Producer: 19930610 In: Nature genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	Linkage relations of the loci for the MN blood group and red cell acid phosphatase. [electronic resource] by Weitkamp, L R Lovrien, E W Olaisen, B Fenger, K Gedde-Dahl, T Sorensen, S A Conneally, P M Bias, W B Ott, J Producer: 19760324 In: Birth defects original article series vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	132.	Linkage group I: multipoint mapping. [electronic resource] by Meyers, D A Conneally, P M Hecht, F Lovrien, E W Magenis, E Merritt, A D Palmer, G C Rivas, M L Wang, L Producer: 19760220 In: Cytogenetics and cell genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	Cooperative study of hospital frequency and character of transient ischemic attacks. III. Variations in treatment. [electronic resource] by Haerer, A F Gotshall, R A Conneally, P M Dyken, M L Poskanzer, D C Price, T R Swanson, P D Calanchini, P R Producer: 19770729 In: JAMA vol. 238 Availability: No items available. Save to lists Add to cart (remove)
	134.	Linkage group I: multipoint mapping. [electronic resource] by Meyers, D A Conneally, P M Hecht, F Lovrien, E W Magenis, E Merritt, A D Palmer, C G Rivas, M L Wang, L Producer: 19760324 In: Birth defects original article series vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	135.	Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. [electronic resource] by Takacs, I Koller, D L Peacock, M Christian, J C Hui, S L Conneally, P M Johnston, C C Foroud, T Econs, M J Producer: 20000107 In: The Journal of clinical endocrinology and metabolism vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families. [electronic resource] by Harper, P S Youngman, S Anderson, M A Sarfarazi, M Quarrell, O Tanzi, R Shaw, D Wallace, P Conneally, P M Gusella, J F Producer: 19860128 In: Journal of medical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	137.	Gametic but not somatic instability of CAG repeat length in Huntington's disease. [electronic resource] by MacDonald, M E Barnes, G Srinidhi, J Duyao, M P Ambrose, C M Myers, R H Gray, J Conneally, P M Young, A Penney, J Producer: 19940418 In: Journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	138.	Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset. [electronic resource] by Haines, J L Amos, J Attwood, J Bech-Hansen, N T Burley, M Conneally, P M Connor, J M Fahsold, R Flodman, P Fryer, A Producer: 19910702 In: Annals of the New York Academy of Sciences vol. 615 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	139.	Molecular genetics of Huntington's disease. [electronic resource] by Gusella, J F Gilliam, T C Tanzi, R E MacDonald, M E Cheng, S V Wallace, M Haines, J Conneally, P M Wexler, N S Producer: 19870626 In: Cold Spring Harbor symposia on quantitative biology vol. 51 Pt 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus. [electronic resource] by Allamand, V Broux, O Bourg, N Richard, I Tischfield, J A Hodes, M E Conneally, P M Fardeau, M Jackson, C E Beckmann, J S Producer: 19950803 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 195 results.