Your search returned 12 results.

Results
	1.	A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity. [electronic resource] by Reid, E Dearlove, A M Rhodes, M Rubinsztein, D C Producer: 19991004 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)
	2.	Benign familial infantile convulsions: report of a UK family and confirmation of genetic heterogeneity. [electronic resource] by Baralle, D Dearlove, A M Beach, R Ffrench-Constant, C Reid, E Producer: 20010201 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity. [electronic resource] by Reid, E Dearlove, A M Whiteford, M L Rhodes, M Rubinsztein, D C Producer: 19991130 In: Neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13. [electronic resource] by Reid, E Dearlove, A M Osborn, O Rogers, M T Rubinsztein, D C Producer: 20000330 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate. [electronic resource] by Reid, E Escayg, A Dearlove, A M Meisler, M H Rubinsztein, D C Producer: 20010510 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)
	6.	Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus. [electronic resource] by Ragge, N K Hartley, C Dearlove, A M Walker, J Russell-Eggitt, I Harris, C M Producer: 20030221 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)
	7.	Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13. [electronic resource] by Curtis, D Brett, P Dearlove, A M McQuillin, A Kalsi, G Robertson, M M Gurling, H M D Producer: 20050324 In: Psychiatric genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Coeliac disease: investigation of proposed causal variants in the CTLA4 gene region. [electronic resource] by King, A L Moodie, S J Fraser, J S Curtis, D Reid, E Dearlove, A M Ciclitira, P J Producer: 20040804 In: European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping. [electronic resource] by Ohadi, M Lalloz, M R Sham, P Zhao, J Dearlove, A M Shiach, C Kinsey, S Rhodes, M Layton, D M Producer: 19990310 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	CTLA-4/CD28 gene region is associated with genetic susceptibility to coeliac disease in UK families. [electronic resource] by King, A L Moodie, S J Fraser, J S Curtis, D Reid, E Dearlove, A M Ellis, H J Ciclitira, P J Producer: 20020312 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Coeliac disease: follow-up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11. [electronic resource] by King, A L Fraser, J S Moodie, S J Curtis, D Dearlove, A M Ellis, H J Rosen-Bronson, S Ciclitira, P J Producer: 20011204 In: Annals of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A genome-wide family-based linkage study of coeliac disease. [electronic resource] by King, A L Yiannakou, J Y Brett, P M Curtis, D Morris, M A Dearlove, A M Rhodes, M Rosen-Bronson, S Mathew, C Ellis, H J Ciclitira, P J Producer: 20010517 In: Annals of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)