Your search returned 18 results.

Results
	1.	Loci for autosomal dominant retinitis pigmentosa and dominant cystoid macular dystrophy on chromosome 7p are not allelic. [electronic resource] by Inglehearn, C Keen, T J al-Maghtheh, M Bhattacharya, S Producer: 19941006 In: American journal of human genetics vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	2.	Simple tests for rhodopsin involvement in retinitis pigmentosa. [electronic resource] by Tarttelin, E Al-Maghtheh, M Keen, J Bhattacharya, S Inglehearn, C Producer: 19961010 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)
	3.	RP11 is the second most common locus for dominant retinitis pigmentosa. [electronic resource] by Vithana, E Al-Maghtheh, M Bhattacharya, S S Inglehearn, C F Producer: 19980423 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)
	4.	Rhodopsin mutations in autosomal dominant retinitis pigmentosa. [electronic resource] by al-Maghtheh, M Gregory, C Inglehearn, C Hardcastle, A Bhattacharya, S Producer: 19931028 In: Human mutation vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Two new rhodopsin transversion mutations (L40R; M216K) in families with autosomal dominant retinitis pigmentosa. [electronic resource] by al-Maghtheh, M Inglehearn, C Lunt, P Jay, M Bird, A Bhattacharya, S Producer: 19941010 In: Human mutation vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family. [electronic resource] by al-Maghtheh, M Kim, R Y Hardcastle, A Inglehearn, C Bhattacharya, S S Producer: 19940523 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A large deletion at the 3' end of the rhodopsin gene in an Italian family with a diffuse form of autosomal dominant retinitis pigmentosa. [electronic resource] by Restagno, G Maghtheh, M Bhattacharya, S Ferrone, M Garnerone, S Samuelly, R Carbonara, A Producer: 19930701 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Variation in DNA polymorphisms of the short arm of the human X chromosome: genetic affinity of Parsi from western India. [electronic resource] by al-Maghtheh, M Ray, V Mastana, S S Garralda, M D Bhattacharya, S S Papiha, S S Producer: 19930907 In: Human heredity vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Segregation of a PRKCG mutation in two RP11 families. [electronic resource] by Al-Maghtheh, M Vithana, E N Inglehearn, C F Moore, T Bird, A C Bhattacharya, S S Producer: 19980521 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Evidence for interaction between human PRUNE and nm23-H1 NDPKinase. [electronic resource] by Reymond, A Volorio, S Merla, G Al-Maghtheh, M Zuffardi, O Bulfone, A Ballabio, A Zollo, M Producer: 20000106 In: Oncogene vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype. [electronic resource] by Al-Maghtheh, M Vithana, E Tarttelin, E Jay, M Evans, K Moore, T Bhattacharya, S Inglehearn, C F Producer: 19961121 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	12.	Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5. [electronic resource] by Kim, R Y al-Maghtheh, M Fitzke, F W Arden, G B Jay, M Bhattacharya, S S Bird, A C Producer: 19931207 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q. [electronic resource] by Evans, K al-Maghtheh, M Fitzke, F W Moore, A T Jay, M Inglehearn, C F Arden, G B Bird, A C Producer: 19960104 In: The British journal of ophthalmology vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity. [electronic resource] by Inglehearn, C F Tarttelin, E E Plant, C Peacock, R E al-Maghtheh, M Vithana, E Bird, A C Bhattacharya, S S Producer: 19980326 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)
	15.	Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19. [electronic resource] by al-Maghtheh, M Inglehearn, C F Keen, T J Evans, K Moore, A T Jay, M Bird, A C Bhattacharya, S S Producer: 19940718 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9). [electronic resource] by Inglehearn, C F Keen, T J al-Maghtheh, M Gregory, C Y Jay, M R Moore, A T Bird, A C Bhattacharya, S S Producer: 19940413 In: American journal of human genetics vol. 54 Availability: No items available. Save to lists Add to cart (remove)
	17.	A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. [electronic resource] by Inglehearn, C F Carter, S A Keen, T J Lindsey, J Stephenson, A M Bashir, R al-Maghtheh, M Moore, A T Jay, M Bird, A C Producer: 19930719 In: Nature genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11). [electronic resource] by Vithana, E N Abu-Safieh, L Allen, M J Carey, A Papaioannou, M Chakarova, C Al-Maghtheh, M Ebenezer, N D Willis, C Moore, A T Bird, A C Hunt, D M Bhattacharya, S S Producer: 20011018 In: Molecular cell vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)