Publications by authors named "Bedia Sahin"

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The genetic counseling in a patient affected by choroideremia solved with the whole-exome sequencing approach.
Bedia Sahin, Erik Burton, Okkes Kuybu, Yavuz Sahin, John Brinkley

Indian J Ophthalmol· July 2022

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A Rare Catheter Complication in a Patient With Neuroblastoma: Horner's Syndrome.
Selma Urfalioglu, Can Acipayam, Mete Güler, Bedia Sahin, Meliha Kübra Kütükcü

Ophthalmic Plast Reconstr Surg· March 2021

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A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.
Yavuz Sahin, Olcay Güngör, Akif Ayaz, Gülay Güngör, Bedia Sahin

Brain Dev· February 2017

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