Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Asal, Samir"'
Publikováno v:
In Acta Otorrinolaringologica (English Edition) May-June 2018 69(3):141-148
Publikováno v:
Egyptian Journal of Otolaryngology; 11/29/2023, Vol. 39 Issue 1, p1-8, 8p
Publikováno v:
In Egyptian Journal of Ear, Nose, Throat and Allied Sciences March 2015 16(1):75-79
Publikováno v:
Egyptian Journal of Otolaryngology; 7/15/2022, Vol. 38 Issue 1, p1-13, 13p
Background & Aim: Hearing loss is the most frequent form of neurosensory deficit in humans. Although the majority of hereditary hearing loss is due to nuclear gene mutations, it has become clear the significant contribution of mitochondrial genes. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6aa3a02117e820775781987824027e9f
https://europepmc.org/articles/PMC4348701/
https://europepmc.org/articles/PMC4348701/
Akademický článek
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Autor:
Asal S; Audiology Department, Alexandria Faculty of Medicine, Alexandria, Egypt., Sobhy O; Audiology Department, Alexandria Faculty of Medicine, Alexandria, Egypt., Balbaa A; Audiology Department, Alexandria Faculty of Medicine, Alexandria, Egypt. Electronic address: amany.balbaa@hotmail.com.
Publikováno v:
Acta otorrinolaringologica espanola [Acta Otorrinolaringol Esp (Engl Ed)] 2018 May - Jun; Vol. 69 (3), pp. 141-148. Date of Electronic Publication: 2017 Aug 31.
Autor:
Fassad MR; Department of Human Genetics, Medical Research Institute, Alexandria University Egypt., Desouky LM; Department of Human Genetics, Medical Research Institute, Alexandria University Egypt., Asal S; Department of Audiology, Alexandria Faculty of Medicine Egypt., Abdalla EM; Department of Human Genetics, Medical Research Institute, Alexandria University Egypt.
Publikováno v:
International journal of molecular epidemiology and genetics [Int J Mol Epidemiol Genet] 2014 Dec 15; Vol. 5 (4), pp. 200-4. Date of Electronic Publication: 2014 Dec 15 (Print Publication: 2014).