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1998, Acta ophthalmologica Scandinavica., ISBN 9788716156839, Volume 226.
Dissertation
Journal Article
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, ISSN 0721-832X, 01/2017, Volume 255, Issue 1, pp. 119 - 125
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 1/2017, Volume 255, Issue 1, pp. 119 - 125
Hereditary congenital cataract varies immensely concerning location and form of the lens opacities. A specific and very rare phenotype is called “ant-egg”... 
Mass spectonometry | Anterior OCT | Medicine & Public Health | Congenital cataract | Proteome | Histology | Ophthalmology | Hereditary | Connexin46
Journal Article
Journal Article
by Simmons, Ruth and Malyuta, Ruslan and Chentsova, Nelli and Medoeva, Antonia and Kruglov, Yuri and Yurchenko, Alexander and Copas, Anew and Porter, Kholoud and del Amo, Julia and Meyer, Laurence and Bucher, Heiner C and Chêne, Geneviève and Hamouda, Osamah and Pillay, Deenan and Prins, Maria and Rosinska, Magda and Sabin, Caroline and Touloumi, Giota and Olson, Ashley and Cartier, Anea and Fradette, Lorraine and Walker, Sarah and Babiker, Abdel and de Luca, Anea and Fisher, Martin and Muga, Roberto and Kelleher, Tony and Cooper, David and Finlayson, Robert and Bloch, Mark and Ramacciotti, Tim and Gelgor, Linda and Smith, Don and Zangerle, Robert and Gill, John and Lutsar, Irja and Wittkop, Linda and Dabis, Francois and Thiebaut, Rodolphe and Costagliola, Dominique and Guiguet, Marguerite and Vanhems, Philippe and Chaix, Marie-Laure and Ghosn, Jade and Boufassa, Faroudy and Kücherer, Claudia and Bartmeyer, Barbara and Sambatakou, Helen and Sipsas, Nikolaos V and Gogos, Charalambos A and Pantazis, Nikos and Katsarou, Olga and Rezza, Giovanni and Dorrucci, Maria and Monforte, Antonella d'Arminio and Geskus, Ronald and van der Helm, Jannie and Schuitemaker, Hanneke and Sannes, Mette and Brubakk, Oddbjorn and Kran, Anne-Marte Bakken and Riise, Anne Margarita Dyrhol and Rosinska, Magdalena and Tor, Jordi and de Olalla, Patricia Garcia and Cayla, Joan and Moreno, Santiago and Monge, Susana and del Romero, Jorge and Pérez-Hoyos, Santiago and Sönnerborg, Anders and Günthard, Hulych and Rickenbach, Martin and Murphy, Gary and Johnson, Anne and Phillips, Anew and Morrison, Charles and Salata, Robert and Mugerwa, Roy and Chipato, Tsungai and Amornkul, Pauli N and Gilmour, Jill and Kamali, Anatoli and Karita, Etienne and Burns, Fiona and Giaquinto, Carlo and Grarup, Jesper and Kirk, Ole and Bailey, Heather and Anne, Alain Volny and Panteleev, Alex and Thorne, Claire and Aboulker, Jean-Pierre and Albert, Jan and Asandi, Silvia and de Wit, Stéphane and Reiss, Peter and Gatell, José and Karpov, Igor and Ledergerber, Bruno and ... and CASCADE Collaboration EuroCoord and CASCADE Collaboration in EuroCoord
PLoS ONE, ISSN 1932-6203, 2015, Volume 10, Issue 8, p. e0137062
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2016, Volume 98, Issue 5, pp. 981 - 992
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 11/2008, Volume 86, Issue 7, pp. 730 - 734
Journal Article
Molecular Vision, ISSN 1090-0535, 09/2006, Volume 12, pp. 1033 - 1039
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 03/2009, Volume 87, Issue 2, pp. 242 - 242
In the November 2008 issue (AOS 86:7), the article by Ulla Edén et al. was not published correctly in the printed issue. Unfortunately, part of the section... 
Wilms tumour | WAGR complex | congenital eye diseases | iris hypoplasia | corneal clouding | PAX6 gene | aniridia | childhood glaucoma | CONGENITAL ANIRIDIA | EYES | TUMOR | GILLESPIE-SYNDROME | KERATOLIMBAL ALLOGRAFT | KERATOPATHY | DYSGENESIS | OPHTHALMOLOGY | PAX6 MUTATIONS | ASSOCIATION
Journal Article