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Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar
Authors:Faiyaz-Ul-Haque M  Zaidi S H E  Al-Mureikhi M S  Peltekova I  Tsui L-C  Teebi A S
Affiliation:Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital &Research Centre, Riyadh, Saudi Arabia,;Program in Genetics and Genomic Biology, Department of Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada,;Department of Genetics Medicine, Weill Cornell Medical College in Qatar, Doha, Qatar,;Department of Medicine, University of Toronto, Toronto, Ontario, Canada,;Department of Pediatrics, Hamad Medical Corp, Doha, Qatar,;The University of Hong Kong, Hong Kong,;and Department of Pediatrics;, and Department of Genetic Medicine, Weill Cornell Medical College in Qatar, Qatar, Education city, Doha, Qatar
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