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	21.	Unusual retinopathy in a child with severe combined immune deficiency. [electronic resource] by Gerth-Kahlert, Christina Tiwari, Amit Hauri-Hohl, Mathias M Hanson, James V M Bahr, Angela Palmowski-Wolfe, Anja Güngör, Tayfun Berger, Wolfgang Producer: 20180326 In: Ophthalmic genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Unfavorable Structural and Functional Outcomes in Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis. [electronic resource] by Jelcic, Ilijas Hanson, James V M Lukas, Sebastian Weber, Konrad P Landau, Klara Pless, Misha Reindl, Markus Weller, Michael Martin, Roland Lutterotti, Andreas Schippling, Sven Producer: 20200615 In: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasia. [electronic resource] by Atac, David Koller, Samuel Hanson, James V M Feil, Silke Tiwari, Amit Bahr, Angela Baehr, Luzy Magyar, István Kottke, Raimund Gerth-Kahlert, Christina Berger, Wolfgang Producer: 20201221 In: Human molecular genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis. [electronic resource] by Vincent, Ajoy Ng, Judith Gerth-Kahlert, Christina Tavares, Erika Maynes, Jason T Wright, Thomas Tiwari, Amit Tumber, Anupreet Li, Shuning Hanson, James V M Bahr, Angela MacDonald, Heather Bähr, Luzy Westall, Carol Berger, Wolfgang Cremers, Frans P M den Hollander, Anneke I Héon, Elise Producer: 20170615 In: Investigative ophthalmology & visual science vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations. [electronic resource] by Gerth-Kahlert, Christina Tiwari, Amit Hanson, James V M Batmanabane, Vaishnavi Traboulsi, Elias Pennesi, Mark E Al-Qahtani, Abdullah A Lam, Byron L Heckenlively, John Zweifel, Sandrine A Vincent, Ajoy Fierz, Fabienne Barthelmes, Daniel Branham, Kari Khan, Naheed Bahr, Angela Baehr, Luzy Magyar, István Koller, Samuel Azzarello-Burri, Silvia Niedrist, Dunja Heon, Elise Berger, Wolfgang Producer: 20170803 In: Investigative ophthalmology & visual science vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. [electronic resource] by Pilorge, M Fassier, C Le Corronc, H Potey, A Bai, J De Gois, S Delaby, E Assouline, B Guinchat, V Devillard, F Delorme, R Nygren, G Råstam, M Meier, J C Otani, S Cheval, H James, V M Topf, M Dear, T N Gillberg, C Leboyer, M Giros, B Gautron, S Hazan, J Harvey, R J Legendre, P Betancur, C Producer: 20170925 In: Molecular psychiatry vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)