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	21.	Isolation of probes specific to human chromosomal region 6p21 from immunoselected irradiation-fusion gene transfer hybrids. [electronic resource] by Ragoussis, J Jones, T A Sheer, D Shrimpton, A E Goodfellow, P N Trowsdale, J Ziegler, A Producer: 19911017 In: Genomics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikely. [electronic resource] by Barron, L Curtis, A Shrimpton, A E Holloway, S May, H Snell, R G Brock, D J Producer: 19911108 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Prenatal diagnosis for the cystic fibrosis mutation 1717-1, G-->A using arms. [electronic resource] by Miedzybrodzka, Z H Kelly, K F Davidson, M Little, S Shrimpton, A E Dean, J C Haites, N E Producer: 19930204 In: Prenatal diagnosis vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Retrovirus-like features and site specific insertions of a transposable element, tom, in Drosophila ananassae. [electronic resource] by Tanda, S Shrimpton, A E Chueh, L L Itayama, H Matsubayashi, H Saigo, K Tobari, Y N Langley, C H Producer: 19890306 In: Molecular & general genetics : MGG vol. 214 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Cognitive deficits associated with a recently reported familial neurodegenerative disease: familial encephalopathy with neuroserpin inclusion bodies. [electronic resource] by Bradshaw, C B Davis, R L Shrimpton, A E Holohan, P D Rea, C B Fieglin, D Kent, P Collins, G H Producer: 20011004 In: Archives of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Risk calculation in retinitis pigmentosa. [electronic resource] by Holloway, S M Strain, L Shrimpton, A E Wright, A F Aldred, M A Brosnahan, D Hammer, H Jay, M Brock, D J Producer: 19911121 In: American journal of human genetics vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	27.	A mutation in CFTR produces different phenotypes depending on chromosomal background. [electronic resource] by Kiesewetter, S Macek, M Davis, C Curristin, S M Chu, C S Graham, C Shrimpton, A E Cashman, S M Tsui, L C Mickle, J Producer: 19940204 In: Nature genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Familial encephalopathy with neuroserpin inclusion bodies. [electronic resource] by Davis, R L Holohan, P D Shrimpton, A E Tatum, A H Daucher, J Collins, G H Todd, R Bradshaw, C Kent, P Feiglin, D Rosenbaum, A Yerby, M S Shaw, C M Lacbawan, F Lawrence, D A Producer: 19991228 In: The American journal of pathology vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Familial dementia caused by polymerization of mutant neuroserpin. [electronic resource] by Davis, R L Shrimpton, A E Holohan, P D Bradshaw, C Feiglin, D Collins, G H Sonderegger, P Kinter, J Becker, L M Lacbawan, F Krasnewich, D Muenke, M Lawrence, D A Yerby, M S Shaw, C M Gooptu, B Elliott, P R Finch, J T Carrell, R W Lomas, D A Producer: 19991019 In: Nature vol. 401 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)