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	61.	The EUROGEM map of human chromosome 9. [electronic resource] by Attwood, J Vergnaud, G Lush, M L Rubinsztein, D C Goudie, D Ferguson-Smith, M Povey, S Producer: 19950227 In: European journal of human genetics : EJHG vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	62.	Genetic associations with clinical characteristics in bipolar affective disorder and recurrent unipolar depressive disorder. [electronic resource] by Ho, L W Furlong, R A Rubinsztein, J S Walsh, C Paykel, E S Rubinsztein, D C Producer: 20000907 In: American journal of medical genetics vol. 96 Availability: No items available. Save to lists Add to cart (remove)
	63.	An empirical exploration of the (delta mu)2 genetic distance for 213 human microsatellite markers. [electronic resource] by Cooper, G Amos, W Bellamy, R Siddiqui, M R Frodsham, A Hill, A V Rubinsztein, D C Producer: 20001002 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Homozygotes and heterozygotes for ciliary neurotrophic factor null alleles do not show earlier onset of Huntington's disease. [electronic resource] by Rubinsztein, D C Leggo, J Chiano, M Korn, S Dodge, A Norbury, G Rosser, E Craufurd, D Producer: 19971010 In: Neurology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years. [electronic resource] by Tysoe, C Robinson, D Brayne, C Dening, T Paykel, E S Huppert, F A Rubinsztein, D C Producer: 19970326 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes. [electronic resource] by Rubinsztein, D C Leggo, J Coetzee, G A Irvine, R A Buckley, M Ferguson-Smith, M A Producer: 19960214 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK. [electronic resource] by Leggo, J Dalton, A Morrison, P J Dodge, A Connarty, M Kotze, M J Rubinsztein, D C Producer: 19980204 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorder. [electronic resource] by Rubinsztein, D C Leggo, J Crow, T J DeLisi, L E Walsh, C Jain, S Paykel, E S Producer: 19970123 In: American journal of medical genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class. [electronic resource] by Yip, A G Dürr, A Marchuk, D A Ashley-Koch, A Hentati, A Rubinsztein, D C Reid, E Producer: 20030930 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Chylomicron remnant clearance from the plasma is normal in familial hypercholesterolemic homozygotes with defined receptor defects. [electronic resource] by Rubinsztein, D C Cohen, J C Berger, G M van der Westhuyzen, D R Coetzee, G A Gevers, W Producer: 19901121 In: The Journal of clinical investigation vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Identification and properties of the proline664-leucine mutant LDL receptor in South Africans of Indian origin. [electronic resource] by Rubinsztein, D C Coetzee, G A Marais, A D Leitersdorf, E Seftel, H C van der Westhuyzen, D R Producer: 19930119 In: Journal of lipid research vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	72.	No association of a functional polymorphism in the dopamine D2 receptor promoter region with bipolar or unipolar affective disorders. [electronic resource] by Furlong, R A Coleman, T A Ho, L Rubinsztein, J S Walsh, C Paykel, E S Rubinsztein, D C Producer: 19981215 In: American journal of medical genetics vol. 81 Availability: No items available. Save to lists Add to cart (remove)
	73.	A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder cases. [electronic resource] by Furlong, R A Ho, L W Rubinsztein, J S Michael, A Walsh, C Paykel, E S Rubinsztein, D C Producer: 20000208 In: Neuroscience letters vol. 277 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100. [electronic resource] by Rubinsztein, D C Raal, F J Seftel, H C Pilcher, G Coetzee, G A van der Westhuyzen, D R Producer: 19930730 In: Arteriosclerosis and thrombosis : a journal of vascular biology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease. [electronic resource] by Tysoe, C Whittaker, J Xuereb, J Cairns, N J Cruts, M Van Broeckhoven, C Wilcock, G Rubinsztein, D C Producer: 19980304 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Autosomal dominant polycystic kidney disease unlinked to the PKD1 and PKD2 loci presenting as familial cerebral aneurysm. [electronic resource] by McConnell, R S Rubinsztein, D C Fannin, T F McKinstry, C S Kelly, B Bailey, I C Hughes, A E Producer: 20011025 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Presenilin-1 intron 8 polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's disease. [electronic resource] by Tysoe, C Whittaker, J Cairns, N J Atkinson, P F Harrington, C R Xuereb, J Wilcock, G Rubinsztein, D C Producer: 19970422 In: Neuroscience letters vol. 222 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	Apo E genotypes and risk of dementia in Down syndrome. [electronic resource] by Rubinsztein, D C Hon, J Stevens, F Pyrah, I Tysoe, C Huppert, F A Easton, D F Holland, A J Producer: 19991101 In: American journal of medical genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorder. [electronic resource] by Kirk, R Furlong, R A Amos, W Cooper, G Rubinsztein, J S Walsh, C Paykel, E S Rubinsztein, D C Producer: 19990820 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	80.	Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly. [electronic resource] by Seguin, S J Morelli, F F Vinet, J Amore, D De Biasi, S Poletti, A Rubinsztein, D C Carra, S Producer: 20150714 In: Cell death and differentiation vol. 21 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 124 results.