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	1.	Classification of rheumatoid arthritis: the importance of including data from the siblings. [electronic resource] by Walker, D J Stephenson, A M Griffiths, I D Roberts, D F Producer: 19871201 In: Genetic epidemiology vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Intravenous methylprednisolone in the treatment of Graves' ophthalmopathy. [electronic resource] by Kendall-Taylor, P Crombie, A L Stephenson, A M Hardwick, M Hall, K Producer: 19890331 In: BMJ (Clinical research ed.) vol. 297 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Linkage studies of HLA and rheumatoid arthritis in multicase families. [electronic resource] by Walker, D J Burn, J Griffiths, I D Roberts, D F Stephenson, A M Producer: 19870316 In: Arthritis and rheumatism vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Prediction of remission after antithyroid drug treatment in Graves' disease. [electronic resource] by Young, E T Steel, N R Taylor, J J Stephenson, A M Stratton, A Holcombe, M Kendall-Taylor, P Producer: 19881123 In: The Quarterly journal of medicine vol. 66 Availability: No items available. Save to lists Add to cart (remove)
	5.	A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13. [electronic resource] by Healy, E Holmes, S C Belgaid, C E Stephenson, A M Mclean, W H Rees, J L Munro, C S Producer: 19960708 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: further locus heterogeneity in adRP. [electronic resource] by Bashir, R Inglehearn, C F Keen, T J Lindsey, J Atif, U Carter, S A Stephenson, A M Jackson, A Jay, M Bird, A C Producer: 19921222 In: Genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity. [electronic resource] by Birch-Machin, M A Healy, E Turner, R Haldane, F Belgaid, C E Darlington, S Stephenson, A M Munro, C Messenger, A G Rees, J L Producer: 19971119 In: The British journal of dermatology vol. 137 Availability: No items available. Save to lists Add to cart (remove)
	8.	A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. [electronic resource] by Inglehearn, C F Carter, S A Keen, T J Lindsey, J Stephenson, A M Bashir, R al-Maghtheh, M Moore, A T Jay, M Bird, A C Producer: 19930719 In: Nature genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Point mutation in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five families. [electronic resource] by Korge, B P Healy, E Traupe, H Pünter, C Mauch, C Hamm, H Birch-Machin, M A Belgaid, C E Stephenson, A M Holmes, S C Darlington, S Messenger, A G Rees, J L Munro, C S Producer: 19990909 In: Experimental dermatology vol. 8 Availability: No items available. Save to lists Add to cart (remove)