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	81.	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)
	82.	Three sequence polymorphisms in the PDC gene. [electronic resource] by Mansergh, F C Jordan, S A Farrar, G J Kumar-Singh, R Gal, A Bhattacharya, S Humphries, P Producer: 19950404 In: Human molecular genetics vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	83.	The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533. [electronic resource] by Li, Y Müller, B Fuhrmann, C van Nouhuys, C E Laqua, H Humphries, P Schwinger, E Gal, A Producer: 19921028 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	84.	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)
	85.	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)
	86.	Recurrence of Philadelphia chromosome-positive leukemia in donor cells after marrow transplantation for chronic granulocytic leukemia: confirmation by microsatellite studies. [electronic resource] by McCann, S R Lawler, M Humphries, P Bacigalupo, A Podesta, M Frassoni, F Van Lint, M T Marmont, A Producer: 19920619 In: Blood vol. 79 Availability: No items available. Save to lists Add to cart (remove)
	87.	Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contig. [electronic resource] by McGuire, R E Jordan, S A Braden, V V Bouffard, G G Humphries, P Green, E D Daiger, S P Producer: 19960917 In: Genome research vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	MRI evaluation of lumbar spine flexion and extension in asymptomatic individuals. [electronic resource] by Edmondston, S J Song, S Bricknell, R V Davies, P A Fersum, K Humphries, P Wickenden, D Singer, K P Producer: 20001113 In: Manual therapy vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	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)
	90.	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)
	91.	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)
	92.	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)
	93.	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)
	94.	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)
	95.	The EUROGEM map of human chromosome 6. [electronic resource] by Terrenato, L Jodice, C Blasi, P Loizedda, A Contu, L Buard, J Vergnaud, G Humphries, P Kumar-Singh, R Massart, C Producer: 19950227 In: European journal of human genetics : EJHG vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	96.	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)
	97.	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)
	98.	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)
	99.	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)
	100.	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)

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Your search returned 117 results.