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	3981.	Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1. [electronic resource] by Downes, S M Holder, G E Fitzke, F W Payne, A M Warren, M J Bhattacharya, S S Bird, A C Producer: 20010125 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 119 Availability: No items available. Save to lists Add to cart (remove)
	3982.	[Heredity of congenital deficiencies in color vision]. [electronic resource] by François, J De Bie, S Verriest, G Matton, M T Producer: 19740429 In: Acta geneticae medicae et gemellologiae vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3983.	Reversible color vision loss in occupational exposure to metallic mercury. [electronic resource] by Cavalleri, A Gobba, F Producer: 19980611 In: Environmental research vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3984.	Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase. [electronic resource] by Gregory-Evans, K Kelsell, R E Gregory-Evans, C Y Downes, S M Fitzke, F W Holder, G E Simunovic, M Mollon, J D Taylor, R Hunt, D M Bird, A C Moore, A T Producer: 20000128 In: Ophthalmology vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3985.	Molecular basis of an inherited form of incomplete achromatopsia. [electronic resource] by Tränkner, Dimitri Jägle, Herbert Kohl, Susanne Apfelstedt-Sylla, Eckart Sharpe, Lindsay T Kaupp, U Benjamin Zrenner, Eberhart Seifert, Reinhard Wissinger, Bernd Producer: 20040130 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3986.	Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A). [electronic resource] by Jiang, Li Katz, Bradley J Yang, Zhenglin Zhao, Yu Faulkner, Nathan Hu, Jianbin Baird, Jennifer Baehr, Wolfgang Creel, Donnell J Zhang, Kang Producer: 20051103 In: Molecular vision vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	3987.	Voriconazole, but not terbinafine, markedly reduces alfentanil clearance and prolongs its half-life. [electronic resource] by Saari, Teijo I Laine, Kari Leino, Kari Valtonen, Mika Neuvonen, Pertti J Olkkola, Klaus T Producer: 20070110 In: Clinical pharmacology and therapeutics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3988.	Toxic risks and nutritional benefits of traditional diet on near visual contrast sensitivity and color vision in the Brazilian Amazon. [electronic resource] by Fillion, Myriam Lemire, Mélanie Philibert, Aline Frenette, Benoît Weiler, Hope Alberta Deguire, Jason Robert Guimarães, Jean Remy Davée Larribe, Fabrice Barbosa, Fernando Mergler, Donna Producer: 20140205 In: Neurotoxicology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3989.	[Pathology of color vision. Practical diagnosis. Clinical significance and socio-occupational applications]. [electronic resource] by Perdriel, G Lanthony, P Chevaleraud, J Producer: 19760320 In: Bulletin des societes d'ophtalmologie de France vol. Spec No Availability: No items available. Save to lists Add to cart (remove)
	3990.	Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography. [electronic resource] by Thiadens, Alberta A H J Somervuo, Ville van den Born, L Ingeborgh Roosing, Susanne van Schooneveld, Mary J Kuijpers, Robert W A M van Moll-Ramirez, Norka Cremers, Frans P M Hoyng, Carel B Klaver, Caroline C W Producer: 20101207 In: Investigative ophthalmology & visual science vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3991.	Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disorders. [electronic resource] by Vincent, Ajoy Wright, Tom Billingsley, Gail Westall, Carol Héon, Elise Producer: 20110729 In: Ophthalmic genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3992.	Novel CNGA3 mutations in Chinese patients with achromatopsia. [electronic resource] by Liang, Xiaofang Dong, Fangtian Li, Hui Li, Huajin Yang, Lizhu Sui, Ruifang Producer: 20150528 In: The British journal of ophthalmology vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3993.	Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence. [electronic resource] by Sumaroka, Alexander Garafalo, Alexandra V Semenov, Evelyn P Sheplock, Rebecca Krishnan, Arun K Roman, Alejandro J Jacobson, Samuel G Cideciyan, Artur V Producer: 20191206 In: Investigative ophthalmology & visual science vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3994.	Neurological and neurophysiological examinations on workers with chronic poisoning by 2,3,7,8-TCDD: follow-up 35 years after exposure. [electronic resource] by Urban, P Pelclová, D Lukás, E Kupka, K Preiss, J Fenclová, Z Smerhovský, Z Producer: 20070223 In: European journal of neurology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3995.	Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia. [electronic resource] by Azam, Maleeha Collin, Rob W J Shah, Syed Tahir Abbas Shah, Aftab Ali Khan, Muhammad Imran Hussain, Alamdar Sadeque, Ahmed Strom, Tim M Thiadens, Alberta A H J Roosing, Susanne den Hollander, Anneke I Cremers, Frans P M Qamar, Raheel Producer: 20100825 In: Molecular vision vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	3996.	Chromatic pupillometry dissects function of the three different light-sensitive retinal cell populations in RPE65 deficiency. [electronic resource] by Lorenz, Birgit Strohmayr, Elisabeth Zahn, Steffen Friedburg, Christoph Kramer, Martin Preising, Markus Stieger, Knut Producer: 20121129 In: Investigative ophthalmology & visual science vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3997.	Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia. [electronic resource] by Li, Fen-Fen Huang, Xiu-Feng Chen, Jie Yu, Xu-Dong Zheng, Mei-Qin Lu, Fan Jin, Zi-Bing Gan, De-Kang Producer: 20160726 In: Journal of translational medicine vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3998.	A rapid method for the measurement of sex hormone binding globulin capacity of sera. [electronic resource] by Rudd, B T Duignan, N M London, D R Producer: 19750808 In: Clinica chimica acta; international journal of clinical chemistry vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3999.	Carcinoma-associated retinopathy in a young teenager with immature teratoma of the ovary. [electronic resource] by Turaka, Kiran Kietz, Daniel Krishnamurti, Lakshmanan Mitchell, Ellen Scanga, Hannah Fu, Valeria L N Sylvester, Christin Producer: 20150330 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4000.	A Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3. [electronic resource] by Hassall, Mark M Barnard, Alun R Orlans, Harry O McClements, Michelle E Charbel Issa, Peter Aslam, Sher A MacLaren, Robert E Producer: 20190524 In: Investigative ophthalmology & visual science vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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