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	41.	First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypes. [electronic resource] by Curtis, A Strain, L Mennie, M Holloway, S Raeburn, J A Besley, G T Brock, D J Producer: 19890203 In: Prenatal diagnosis vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation. [electronic resource] by Strain, L Porteous, M E Gosden, C M Ellis, P M Neilson, J P Bonthron, D T Producer: 19941110 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Structure and mutation analysis of the gene encoding DNA fragmentation factor 40 (caspase-activated nuclease), a candidate neuroblastoma tumour suppressor gene. [electronic resource] by Judson, H van Roy, N Strain, L Vandesompele, J Van Gele, M Speleman, F Bonthron, D T Producer: 20000614 In: Human genetics vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. [electronic resource] by FitzPatrick, D R Strain, L Thomas, A E Barr, D G Todd, A Smith, N M Scobie, W G Producer: 19971006 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)
	45.	Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family. [electronic resource] by Kovács, G G Ertsey, C Majtényi, C Jelencsik, I László, L Flicker, H Strain, L Szirmai, I Budka, H Producer: 20010816 In: Journal of neurology, neurosurgery, and psychiatry vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	A novel atypical 22q11.2 distal deletion in father and son. [electronic resource] by Garcia-Miñaur, S Fantes, J Murray, R S Porteous, M E M Strain, L Burns, J E Stephen, J Warner, J P Producer: 20021213 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)
	47.	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)
	48.	Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation. [electronic resource] by Saland, J M Emre, S H Shneider, B L Benchimol, C Ames, S Bromberg, J S Remuzzi, G Strain, L Goodship, T H J Producer: 20061128 In: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts. [electronic resource] by Fremeaux-Bacchi, V Kemp, E J Goodship, J A Dragon-Durey, M-A Strain, L Loirat, C Deng, H-W Goodship, T H J Producer: 20060717 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	The normal population distribution of PRNP codon 129 polymorphism. [electronic resource] by Nurmi, M H Bishop, M Strain, L Brett, F McGuigan, C Hutchison, M Farrell, M Tilvis, R Erkkilä, S Simell, O Knight, R Haltia, M Producer: 20040130 In: Acta neurologica Scandinavica vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Heterogeneity analysis in 40 X-linked retinitis pigmentosa families. [electronic resource] by Teague, P W Aldred, M A Jay, M Dempster, M Harrison, C Carothers, A D Hardwick, L J Evans, H J Strain, L Brock, D J Producer: 19940729 In: American journal of human genetics vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	52.	Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850T. [electronic resource] by Waters, A M Pappworth, I Marchbank, K Bockenhauer, D Tullus, K Pickering, M C Strain, L Sebire, N Shroff, R Marks, S D Goodship, T H J Rees, L Producer: 20100304 In: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantation. [electronic resource] by Brown, J H Tellez, J Wilson, V Mackie, I J Scully, M Tredger, M M Moore, I McDougall, N I Strain, L Marchbank, K J Sheerin, N S O'Grady, J Harris, C L Goodship, T H J Producer: 20121012 In: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)