Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Doulati, M."'
Autor:
Hosseinipour, A., Chaleshtori, M. H., Sasanfar, R., Farhud, D. D., Tolooi, A., Doulati, M., Rad, L. H., Mostafa Montazer zohour, Ghadami, M.
Publikováno v:
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 47-50 (2005)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 34, Iss 1 (2005)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 34, Iss 1 (2005)
Autosomal recessive and sporadic non-syndromic hearing loss (ARSNSHL) is the major form of hereditary deafness.Mutations in the GJB2 gene encoding the gap-junction protein Connexin 26 have been identified to be highly associated with ARSNSHL. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1e653603819d8baf36677b6f89918450
http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/908.pdf&manuscript_id=908
http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/908.pdf&manuscript_id=908
Publikováno v:
Paramedical Sciences & Military Health. 2024, Vol. 18 Issue 3, p1-9. 9p.
Autor:
Koohiyan, Mahbobeh1 (AUTHOR) mkouhiyan@gmail.com, Koohian, Farideh2 (AUTHOR), Azadegan‐Dehkordi, Fatemeh1 (AUTHOR)
Publikováno v:
Annals of Human Genetics. Mar2020, Vol. 84 Issue 2, p107-113. 7p.
Autor:
طهماسبی, پریسا1, کاظمی نژاد, سیدرضا1 kazemi_reza@yahoo.de, طباطبایی فر, محمدامین2, محمدی اصل, جواد3, صاکی, نادر4
Publikováno v:
Arak Medical University Journal. 2016, Vol. 19 Issue 6, p68-77. 10p.
Publikováno v:
Indian Journal of Forensic Medicine & Toxicology; Jul-Sep2018, Vol. 12 Issue 3, p217-222, 6p
Publikováno v:
European Archives of Oto-Rhino-Laryngology; May2016, Vol. 273 Issue 5, p1161-1165, 5p
Autor:
Daneshi, A, Hassanzadeh, S, Emamdjomeh, H, Mohammadi, S H, Arzhangi, S, Farhadi, M, Najmabadi, H
Publikováno v:
Journal of Laryngology & Otology; May2011, Vol. 125 Issue 5, p455-459, 5p