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	21.	Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. [electronic resource] by Farrar, G J Kenna, P Jordan, S A Kumar-Singh, R Humphries, M M Sharp, E M Sheils, D Humphries, P Producer: 19921217 In: Genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21. [electronic resource] by Farrar, G J McWilliam, P Sharp, E M Kenna, P Bradley, D G Humphries, M M McConnell, D J Humphries, P Producer: 19900309 In: Genomics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin. [electronic resource] by Jordan, S A Farrar, G J Kumar-Singh, R Kenna, P Humphries, M M Allamand, V Sharp, E M Humphries, P Producer: 19920402 In: American journal of human genetics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	24.	Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. [electronic resource] by Farrar, G J Kenna, P Jordan, S A Kumar-Singh, R Humphries, M M Sharp, E M Sheils, D Humphries, P Producer: 19930414 In: Genomics vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	25.	Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene. [electronic resource] by Mansergh, F C Millington-Ward, S Kennan, A Kiang, A S Humphries, M Farrar, G J Humphries, P Kenna, P F Producer: 20000405 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)
	26.	A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucoma. [electronic resource] by Kennan, A M Mansergh, F C Fingert, J H Clark, T Ayuso, C Kenna, P F Humphries, P Farrar, G J Producer: 19990204 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa. [electronic resource] by Horn, M Humphries, P Kunisch, M Marchese, C Apfelstedt-Sylla, E Fugi, L Zrenner, E Kenna, P Gal, A Farrar, J Producer: 19930225 In: Human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. [electronic resource] by Farrar, G J Kenna, P Jordan, S A Kumar-Singh, R Humphries, M M Sharp, E M Sheils, D M Humphries, P Producer: 19920121 In: Nature vol. 354 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6. [electronic resource] by Farrar, G J Jordan, S A Kenna, P Humphries, M M Kumar-Singh, R McWilliam, P Allamand, V Sharp, E Humphries, P Producer: 19920313 In: Genomics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. [electronic resource] by al-Jandal, N Farrar, G J Kiang, A S Humphries, M M Bannon, N Findlay, J B Humphries, P Kenna, P F Producer: 19990311 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene. [electronic resource] by McNally, N Kenna, P Humphries, M M Hobson, A H Khan, N W Bush, R A Sieving, P A Humphries, P Farrar, G J Producer: 19990816 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Apoptotic photoreceptor death in the rhodopsin knockout mouse in the presence and absence of c-fos. [electronic resource] by Hobson, A H Donovan, M Humphries, M M Tuohy, G McNally, N Carmody, R Cotter, T Farrar, G J Kenna, P F Humphries, P Producer: 20001018 In: Experimental eye research vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus. [electronic resource] by Bradley, D G Farrar, G J Sharp, E M Kenna, P Humphries, M M McConnell, D J Daiger, S P McWilliam, P Humphries, P Producer: 19890503 In: American journal of human genetics vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	34.	Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin. [electronic resource] by Farrar, G J Kenna, P Redmond, R Shiels, D McWilliam, P Humphries, M M Sharp, E M Jordan, S Kumar-Singh, R Humphries, P Producer: 19920313 In: Genomics vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	35.	Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups. [electronic resource] by Daiger, S P Humphries, M M Giesenschlag, N Sharp, E McWilliam, P Farrer, J Bradley, D Kenna, P McConnell, D J Sparkes, R S Producer: 19891207 In: Cytogenetics and cell genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3. [electronic resource] by McWilliam, P Farrar, G J Kenna, P Bradley, D G Humphries, M M Sharp, E M McConnell, D J Lawler, M Sheils, D Ryan, C Producer: 19900309 In: Genomics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Epidermolysis bullosa: evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex form. [electronic resource] by Humphries, M M Sheils, D Lawler, M Farrar, G J McWilliam, P Kenna, P Bradley, D G Sharp, E M Gaffney, E F Young, M Producer: 19900813 In: Genomics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from Europe. [electronic resource] by Farrar, G J Kenna, P Redmond, R McWilliam, P Bradley, D G Humphries, M M Sharp, E M Inglehearn, C F Bashir, R Jay, M Producer: 19901226 In: American journal of human genetics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	39.	A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex. [electronic resource] by Humphries, M M Sheils, D M Farrar, G J Kumar-Singh, R Kenna, P F Mansergh, F C Jordan, S A Young, M Humphries, P Producer: 19930521 In: Human mutation vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity. [electronic resource] by Farrar, G J McWilliam, P Bradley, D G Kenna, P Lawler, M Sharp, E M Humphries, M M Eiberg, H Conneally, P M Trofatter, J A Producer: 19910509 In: Genomics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 48 results.