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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 1, 2023. (Total: 223516Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Corneal Opacity and CYP1B1[original query]
CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited.
Ophthalmology 2011 Sep 118 (9): 1865-73.
Kelberman Daniel, Islam Lily, Jacques Thomas S, Russell-Eggitt Isabelle, Bitner-Glindzicz Maria, Khaw Peng T, Nischal Ken K, Sowden Jane
CYP1B1 genotype influences the phenotype in primary congenital glaucoma and surgical treatment.
The British journal of ophthalmology 2014 Feb 98 (2): 246-51.
Chen Xueli, Chen Yuhong, Wang Li, Jiang Deke, Wang Wenzhang, Xia Mingying, Yu Long, Sun Xinghu
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients.
Clinical genetics 2022 2 101 (5-6): 494-506.
Chesneau Bertrand, Aubert-Mucca Marion, Fremont Félix, Pechmeja Jacmine, Soler Vincent, Isidor Bertrand, Nizon Mathilde, Dollfus Hélène, Kaplan Josseline, Fares-Taie Lucas, Rozet Jean-Michel, Busa Tiffany, Lacombe Didier, Naudion Sophie, Amiel Jeanne, Rio Marlène, Attie-Bitach Tania, Lesage Cécile, Thouvenin Dominique, Odent Sylvie, Morel Godelieve, Vincent-Delorme Catherine, Boute Odile, Vanlerberghe Clémence, Dieux Anne, Boussion Simon, Faivre Laurence, Pinson Lucile, Laffargue Fanny, Le Guyader Gwenaël, Le Meur Guylène, Prieur Fabienne, Lambert Victor, Laudier Beatrice, Cottereau Edouard, Ayuso Carmen, Corton-Pérez Marta, Bouneau Laurence, Le Caignec Cédric, Gaston Véronique, Jeanton-Scaramouche Claire, Dupin-Deguine Delphine, Calvas Patrick, Chassaing Nicolas, Plaisancié Jul
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