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Ophthalmologic abnormalities in a de novo terminal 6q deletion.
Abu-Amero KK, Hellani A, Salih MA, Al Hussain A, al Obailan M, Zidan G, Alorainy IA, Bosley TM. Abu-Amero KK, et al. Among authors: bosley tm. Ophthalmic Genet. 2010 Mar;31(1):1-11. doi: 10.3109/13816810903312535. Ophthalmic Genet. 2010. PMID: 20141352
Ophthalmologic observations in a patient with partial mosaic trisomy 8.
Abu-Amero KK, Kondkar AA, Salih MA, Al-Husain M, Al Shammari M, Zeidan G, Oystreck DT, Hellani AM, Kentab AY, Bosley TM. Abu-Amero KK, et al. Among authors: bosley tm. Ophthalmic Genet. 2013 Dec;34(4):249-53. doi: 10.3109/13816810.2012.762933. Epub 2013 Feb 13. Ophthalmic Genet. 2013. PMID: 23406309
CCDD Phenotype Associated with a Small Chromosome 2 Deletion.
Abu-Amero KK, Bosley TM, Kondkar AA, Oystreck DT, Khan AO. Abu-Amero KK, et al. Among authors: bosley tm. Semin Ophthalmol. 2015;30(5-6):435-42. doi: 10.3109/08820538.2013.874474. Epub 2014 Jan 29. Semin Ophthalmol. 2015. PMID: 24475916
188 results