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	21.	Molecular genetic analysis of von Hippel-Lindau disease. [electronic resource] by Richards, F M Webster, A R McMahon, R Woodward, E R Rose, S Maher, E R Producer: 19980813 In: Journal of internal medicine vol. 243 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patients. [electronic resource] by Grayson, C Chapple, J P Willison, K R Webster, A R Hardcastle, A J Cheetham, M E Producer: 20020312 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)
	23.	Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene. [electronic resource] by Sergouniotis, P I Davidson, A E Sehmi, K Webster, A R Robson, A G Moore, A T Producer: 20111020 In: Eye (London, England) vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health Service. [electronic resource] by Khan, K N Chana, R Ali, N Wright, G Webster, A R Moore, A T Michaelides, M Producer: 20170613 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance. [electronic resource] by Vaclavik, V Chakarova, C Bhattacharya, S S Robson, A G Holder, G E Bird, A C Webster, A R Producer: 20080219 In: The British journal of ophthalmology vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	A detailed phenotypic description of autosomal dominant cone dystrophy due to a de novo mutation in the GUCY2D gene. [electronic resource] by Mukherjee, R Robson, A G Holder, G E Stockman, A Egan, C A Moore, A T Webster, A R Producer: 20141024 In: Eye (London, England) vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. [electronic resource] by Robson, A G Saihan, Z Jenkins, S A Fitzke, F W Bird, A C Webster, A R Holder, G E Producer: 20060413 In: The British journal of ophthalmology vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration. [electronic resource] by Stone, E M Webster, A R Vandenburgh, K Streb, L M Hockey, R R Lotery, A J Sheffield, V C Producer: 19981221 In: Nature genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Functional observations in vitamin A deficiency: diagnosis and time course of recovery. [electronic resource] by McBain, V A Egan, C A Pieris, S J Supramaniam, G Webster, A R Bird, A C Holder, G E Producer: 20070508 In: Eye (London, England) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Isolated foveal retinoschisis as a cause of visual loss in young females. [electronic resource] by Kabanarou, S A Holder, G E Bird, A C Webster, A R Stanga, P E Vickers, S Harney, B A Producer: 20030718 In: The British journal of ophthalmology vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations. [electronic resource] by Maher, E R Webster, A R Richards, F M Green, J S Crossey, P A Payne, S J Moore, A T Producer: 19960925 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors. [electronic resource] by Prowse, A H Webster, A R Richards, F M Richard, S Olschwang, S Resche, F Affara, N A Maher, E R Producer: 19970508 In: American journal of human genetics vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	33.	Chromosomal assignment of 311 sequences transcribed in human adult testis. [electronic resource] by Jones, M H Zhang, Y Tirosvoutis, K N Davey, P M Webster, A R Walsh, D Spurr, N K Affara, N A Producer: 19970623 In: Genomics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy. [electronic resource] by Robson, A G Michaelides, M Luong, V A Holder, G E Bird, A C Webster, A R Moore, A T Fitzke, F W Producer: 20080118 In: The British journal of ophthalmology vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	A detailed phenotypic study of "cone dystrophy with supernormal rod ERG". [electronic resource] by Michaelides, M Holder, G E Webster, A R Hunt, D M Bird, A C Fitzke, F W Mollon, J D Moore, A T Producer: 20050509 In: The British journal of ophthalmology vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Diverse clinical phenotypes associated with a nonsense mutation in FAM161A. [electronic resource] by Rose, A M Sergouniotis, P Alfano, G Muspratt-Tucker, N Barton, S Moore, A T Black, G Bhattacharya, S S Webster, A R Producer: 20160606 In: Eye (London, England) vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene. [electronic resource] by Tschernutter, M Jenkins, S A Waseem, N H Saihan, Z Holder, G E Bird, A C Bhattacharya, S S Ali, R R Webster, A R Producer: 20060613 In: The British journal of ophthalmology vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophy. [electronic resource] by Saihan, Z Li, Z Rice, J Rana, N A Ramsden, S Schlottmann, P G Jenkins, S A Blyth, C Black, G C McKie, N Webster, A R Producer: 20090914 In: Molecular vision vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	39.	ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy. [electronic resource] by Michaelides, M Chen, L L Brantley, M A Andorf, J L Isaak, E M Jenkins, S A Holder, G E Bird, A C Stone, E M Webster, A R Producer: 20071206 In: The British journal of ophthalmology vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts. [electronic resource] by Arora, A Minogue, P J Liu, X Addison, P K Russel-Eggitt, I Webster, A R Hunt, D M Ebihara, L Beyer, E C Berthoud, V M Moore, A T Producer: 20080403 In: Journal of medical genetics vol. 45 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 46 results.