Author:
Musleh M,Hall G,Lloyd I C,Gillespie R L,Waller S,Douzgou S,Clayton-Smith J,Kehdi E,Black G C M,Ashworth J
Publisher
Springer Science and Business Media LLC
Reference11 articles.
1. Rahi JS, Dezateux C . Measuring and interpreting the incidence of congenital ocular anomalies: lessons from a national study of congenital cataract in the UK. Invest Ophthalmol Vis Sci 2001; 42 (7): 1444–1448.
2. Lloyd IC, Goss-Sampson M, Jeffrey BG, Kriss A, Russell-Eggitt I, Taylor D . Neonatal cataract: aetiology, pathogenesis and management. Eye (Lond) 1992; 6 (Pt 2): 184–196.
3. Wirth MG, Russell-Eggitt IM, Craig JE, Elder JE, Mackey DA . Aetiology of congenital and paediatric cataract in an Australian population. Br J Ophthalmol 2002; 86 (7): 782–786.
4. Gillespie RL, O’Sullivan J, Ashworth J, Bhaskar S, Williams S, Biswas S et al. Personalized diagnosis and management of congenital cataract by next-generation sequencing. Ophthalmology. Ophthalmology 2014; 121 (11):2124–2137 (e1-2).
5. Moreno-Igoa M, Hernandez-Charro B, Bengoa-Alonso A, Perez-Juana-del-Casal A, Romero-Ibarra C, Nieva-Echebarria B et al. KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome. BMC Med Genet 2015; 16: 68.
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