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	1.	Corneal opacities in the Hallermann-Streiff syndrome. [electronic resource] by Roulez, Françoise M Schuil, Josée Meire, Françoise M Producer: 20080708 In: Ophthalmic genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Orbital myositis in a child with linear scleroderma en coup de sabre. [electronic resource] by Roulez, Françoise M Dangoisse, Chantal Dufour, Dominique Meire, Françoise M Producer: 20071106 In: Journal of pediatric ophthalmology and strabismus vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2. [electronic resource] by Abouzeid, Hana Meire, Françoise M Osman, Ihab ElShakankiri, Nihal Bolay, Sylvain Munier, Francis L Schorderet, Daniel F Producer: 20090115 In: Ophthalmology vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy. [electronic resource] by Desir, Julie Moya, Graciela Reish, Orit Van Regemorter, Nicole Deconinck, Hilde David, Karen L Meire, Françoise M Abramowicz, Marc J Producer: 20070521 In: Journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndrome. [electronic resource] by Roulez, Françoise M J Faes, Fran Delbeke, Patricia Van Bogaert, Patrick Rodesch, Georges De Zaeytijd, Julie Depasse, Fanny Coucke, Paul J Meire, Francoise M Producer: 20141230 In: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1. [electronic resource] by Payne, Marielle Yang, Zhenglin Katz, Bradley J Warner, Judith E A Weight, Christopher J Zhao, Yu Pearson, Erik D Treft, Robert L Hillman, Todd Kennedy, Richard J Meire, Francoise M Zhang, Kang Producer: 20041209 In: American journal of ophthalmology vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. [electronic resource] by van Genderen, Maria M Bijveld, Mieke M C Claassen, Yvonne B Florijn, Ralph J Pearring, Jillian N Meire, Francoise M McCall, Maureen A Riemslag, Frans C C Gregg, Ronald G Bergen, Arthur A B Kamermans, Maarten Producer: 20091222 In: American journal of human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)