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Case report of a novel mutation of the EYA1 gene in a patient with branchio-oto-renal syndrome Cover

Case report of a novel mutation of the EYA1 gene in a patient with branchio-oto-renal syndrome

Open Access
|Dec 2016

Authors

L Spahiu

Pediatric Clinic, University Clinical Center of Kosovo, Pristina, Republic of Kosovo

B Merovci

m_besart@hotmail.com

Pediatric Clinic, University Clinical Center of Kosovo, Pristina, Republic of Kosovo

V Ismaili Jaha

Pediatric Clinic, University Clinical Center of Kosovo, Pristina, Republic of Kosovo

A Batalli Këpuska

Pediatric Clinic, University Clinical Center of Kosovo, Pristina, Republic of Kosovo

H Jashari

Pediatric Clinic, University Clinical Center of Kosovo, Pristina, Republic of Kosovo
Language: English
Page range: 91 - 94
Published on: Dec 31, 2016
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2016 L Spahiu, B Merovci, V Ismaili Jaha, A Batalli Këpuska, H Jashari, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.