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	1.	Haze following photorefractive and photoastigmatic refractive keratectomy with the Nidek EC5000 and the Summit ExciMed UV200. [electronic resource] by Goggin, M Kenna, P Lavery, F Producer: 19970617 In: Journal of cataract and refractive surgery vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Retinitis pigmentosa and schizophrenia. [electronic resource] by McDonald, C Kenna, P Larkin, T Producer: 20121002 In: European psychiatry : the journal of the Association of European Psychiatrists vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	New dimensions in macular dystrophies. [electronic resource] by Humphries, P Kenna, P Farrar, G J Producer: 19950426 In: Nature genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	On the molecular genetics of retinitis pigmentosa. [electronic resource] by Humphries, P Kenna, P Farrar, G J Producer: 19920619 In: Science (New York, N.Y.) vol. 256 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Photoastigmatic refractive keratectomy for compound myopic astigmatism with a Nidek laser. [electronic resource] by Goggin, M J Kenna, P F Lavery, F L Producer: 19970627 In: Journal of refractive surgery (Thorofare, N.J. : 1995) vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Giant retinal tear in Usher syndrome type II: coincidence or association? [electronic resource] by Cahill, M T Barry, P J Kenna, P F Producer: 19980619 In: Retina (Philadelphia, Pa.) vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease. [electronic resource] by Humphries, P Farrar, G J Kenna, P McWilliam, P Producer: 19900926 In: Clinical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions. [electronic resource] by Jordan, S A Farrar, G J Kenna, P Humphries, P Producer: 19930610 In: Human mutation vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosa. [electronic resource] by Kumar-Singh, R Kenna, P F Farrar, G J Humphries, P Producer: 19930316 In: Genomics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouse. [electronic resource] by Campbell, M Humphries, M Kennan, A Kenna, P Humphries, P Brankin, B Producer: 20061106 In: Experimental eye research vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A sequence polymorphism in the human peripherin/RDS gene. [electronic resource] by Farrar, G J Kenna, P Jordan, S A Kumar-Singh, R Humphries, P Producer: 19920211 In: Nucleic acids research vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Gene-based therapies for dominantly inherited retinopathies. [electronic resource] by Farrar, G J Millington-Ward, S Chadderton, N Humphries, P Kenna, P F Producer: 20120830 In: Gene therapy vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa. [electronic resource] by Fishman, G A Stone, E M Gilbert, L D Kenna, P Sheffield, V C Producer: 19911112 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A mutation-independent therapeutic strategem for osteogenesis imperfecta. [electronic resource] by Millington-Ward, S O'Neill, B Kiang, A S Humphries, P Kenna, P F Farrar, G J Producer: 20000214 In: Antisense & nucleic acid drug development vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Novel mutations in the TIGR gene in early and late onset open angle glaucoma. [electronic resource] by Mansergh, F C Kenna, P F Ayuso, C Kiang, A S Humphries, P Farrar, G J Producer: 19980429 In: Human mutation vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8). [electronic resource] by Kumar-Singh, R Farrar, G J Mansergh, F Kenna, P Bhattacharya, S Gal, A Humphries, P Producer: 19931004 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family. [electronic resource] by Farrar, G J Findlay, J B Kumar-Singh, R Kenna, P Humphries, M M Sharpe, E Humphries, P Producer: 19930617 In: Human molecular genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locus. [electronic resource] by Jordan, S A del Rio, T Soriano, N Garcia-Sandoval, B Kenna, P Ayuso, C Benitez, J Humphries, P Producer: 19930607 In: Human molecular genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness. [electronic resource] by Kenna, P Mansergh, F Millington-Ward, S Erven, A Kumar-Singh, R Brennan, R Farrar, G J Humphries, P Producer: 19970519 In: The British journal of ophthalmology vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Ribozyme-based therapeutic approaches for autosomal dominant retinitis pigmentosa. [electronic resource] by O'Neill, B Millington-Ward, S O'Reilly, M Tuohy, G Kiang, A S Kenna, P F Humphries, P Farrar, G J Producer: 20000914 In: Investigative ophthalmology & visual science vol. 41 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 48 results.