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	41.	Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q. [electronic resource] by Jordan, S A Farrar, G J Kenna, P Humphries, M M Sheils, D M Kumar-Singh, R Sharp, E M Soriano, N Ayuso, C Benitez, J 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)
	42.	Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy. [electronic resource] by Mansergh, F C Kenna, P F Rudolph, G Meitinger, T Farrar, G J Kumar-Singh, R Scorer, J Hally, A M Mynett-Johnson, L Humphries, M M Producer: 19960403 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa. [electronic resource] by Bleeker-Wagemakers, L M Gal, A Kumar-Singh, R van den Born, L I Li, Y Schwinger, E Sandkuijl, L A Bergen, A A Kenna, P 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)
	44.	Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic background. [electronic resource] by Humphries, M M Kiang, S McNally, N Donovan, M A Sieving, P A Bush, R A Machida, S Cotter, T Hobson, A Farrar, J Humphries, P Kenna, P Producer: 20011226 In: Visual neuroscience vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland. [electronic resource] by Humphries, M M Mansergh, F C Kiang, A S Jordan, S A Sheils, D M Martin, M J Farrar, G J Kenna, P F Young, M M Humphries, P Producer: 19961120 In: Human mutation vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Strategems in vitro for gene therapies directed to dominant mutations. [electronic resource] by Millington-Ward, S O'Neill, B Tuohy, G Al-Jandal, N Kiang, A S Kenna, P F Palfi, A Hayden, P Mansergh, F Kennan, A Humphries, P Farrar, G J Producer: 19980202 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Retinopathy induced in mice by targeted disruption of the rhodopsin gene. [electronic resource] by Humphries, M M Rancourt, D Farrar, G J Kenna, P Hazel, M Bush, R A Sieving, P A Sheils, D M McNally, N Creighton, P Erven, A Boros, A Gulya, K Capecchi, M R Humphries, P Producer: 19970310 In: Nature genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia. [electronic resource] by Greene, C Kealy, J Humphries, M M Gong, Y Hou, J Hudson, N Cassidy, L M Martiniano, R Shashi, V Hooper, S R Grant, G A Kenna, P F Norris, K Callaghan, C K Islam, M dN O'Mara, S M Najda, Z Campbell, S G Pachter, J S Thomas, J Williams, N M Humphries, P Murphy, K C Campbell, M Producer: 20190731 In: Molecular psychiatry vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)