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	1.	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)
	2.	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)
	3.	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)
	4.	Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3q. [electronic resource] by Kumar-Singh, R Wang, H Humphries, P Farrar, G J Producer: 19930310 In: American journal of human genetics vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	5.	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)
	6.	Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophy. [electronic resource] by Mansergh, F Meitinger, T Rodolph, G Humphries, P Farrar, G J 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)
	7.	Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus. [electronic resource] by Kumar-Singh, R Jordan, S A Farrar, G J Humphries, P Producer: 19911202 In: Nucleic acids research vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	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)
	9.	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)
	10.	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)
	11.	Linkage analysis of X linked retinitis pigmentosa in the Irish population. [electronic resource] by Farrar, G J Geraghty, M T Moloney, J M McConnell, D J Humphries, P Producer: 19880616 In: Journal of medical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4). [electronic resource] by Kumar-Singh, R Bradley, D G Farrar, G J Lawler, M Jordan, S A Humphries, P Producer: 19910520 In: Human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4). [electronic resource] by Kumar-Singh, R Bradley, D G Farrar, G J Lawler, M Jordan, S A Humphries, P Producer: 19951120 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	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)
	15.	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)
	16.	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)
	17.	Alu polymorphism in the human type I Keratin (KRT14) gene. [electronic resource] by Humphries, M M Sheils, D M Jordan, S A Farrar, G J Kumar-Singh, R 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)
	18.	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)
	19.	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)
	20.	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)

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Your search returned 47 results.