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	21.	A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28. [electronic resource] by Curtis, A R Lindsay, S Boye, E Clarke, A J Landy, S J Bhattacharya, S S Producer: 19940830 In: European journal of human genetics : EJHG vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome. [electronic resource] by Lindsay, S Curtis, A R Roustan, P Kamakari, S Thiselton, D L Stephenson, A Bhattacharya, S S Producer: 19931022 In: Genomics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25. [electronic resource] by Bui, T D Lako, M Lejeune, S Curtis, A R Strachan, T Lindsay, S Harris, A L Producer: 19970623 In: Gene vol. 189 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Dinucleotide repeat polymorphism at the DXS556 locus. [electronic resource] by Thiselton, D L Kamakari, S Curtis, A R Coleman, M P Davies, K E Lindsay, S Bhattacharya, S Producer: 19930727 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Neuroferritinopathy in a French family with late onset dominant dystonia. [electronic resource] by Chinnery, P F Curtis, A R J Fey, C Coulthard, A Crompton, D Curtis, A Lombés, A Burn, J Producer: 20030805 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)
	26.	X chromosome linkage studies in familial Rett syndrome. [electronic resource] by Curtis, A R Headland, S Lindsay, S Thomas, N S Boye, E Kamakari, S Roustan, P Anvret, M Wahlstrom, J McCarthy, G Producer: 19930305 In: Human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. [electronic resource] by Curtis, A R Fey, C Morris, C M Bindoff, L A Ince, P G Chinnery, P F Coulthard, A Jackson, M J Jackson, A P McHale, D P Hay, D Barker, W A Markham, A F Bates, D Curtis, A Burn, J Producer: 20010816 In: Nature genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. [electronic resource] by Li, Q Y Newbury-Ecob, R A Terrett, J A Wilson, D I Curtis, A R Yi, C H Gebuhr, T Bullen, P J Robson, S C Strachan, T Bonnet, D Lyonnet, S Young, I D Raeburn, J A Buckler, A J Law, D J Brook, J D Producer: 19970128 In: Nature genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)