Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran

Autor: M Hashemzadeh Chaleshtori, M Montazer Zohour, L Hoghooghi Rad, H Pour-Jafari, DD Farhud, M Dolati, K Safa Chaleshtori, R Sasanfar, A Hosseinipour, L Andonian, A Tolouei, M Ghadami, MA Patton

Publikováno v: Iranian Journal of Public Health, Vol 35, Iss 1, Pp 88-91 (2006)

Despite the enormous heterogeneity of genetic hearing loss, mutations in the GJB2 (connexin 26) gene located on “DFNB1” locus (13q12) account for up to 50% of cases of autosomal recessive non-syndromic hearing loss (ARNSHL) in some populations. T

Externí odkaz: https://doaj.org/article/94624327e9134bf5967b9c2cfabddedc

'Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations'

Autor: M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton "

Publikováno v: Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)

Mutations in the GJB2 gene encoding Connexin 26 (Cx26) protein are a major cause for autosomal recessive non syndromic and sporadic deafness in many populations. In this study we have investigated the prevalence of the GJB2 gene mutations using neste

Externí odkaz: https://doaj.org/article/a458d4a14e3543a18e8b538ea71f31ec

'Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations'

Autor: 'M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton \\'

Publikováno v: Iranian Journal of Public Health, Vol 33, Iss 2 (2004)
Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)

Mutations in the GJB2 gene encoding Connexin 26 (Cx26) protein are a major cause for autosomal recessive non syndromic and sporadic deafness in many populations. In this study we have investigated the prevalence of the GJB2 gene mutations using neste

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::071856730eb048591ef9426273e79951
https://ijph.tums.ac.ir/index.php/ijph/article/view/1910

Psychological profile of children with Noonan syndrome.

Autor: DA Lee, S Portnoy, P Hill, C Gillberg, MA Patton

Publikováno v: Developmental Medicine & Child Neurology; Jan2005, Vol. 47 Issue 1, p35-38, 4p

Physiotherapists Both Reproduce and Resist Biomedical Dominance when Working With People With Low Back Pain: A Qualitative Study Towards New Praxis.

Autor: Mescouto K; School of Health and Rehabilitation Sciences, 1974The University of Queensland, Brisbane, QLD, Australia., Olson RE; School of Social Science, 144911The University of Queensland, Brisbane, QLD, Australia., Hodges PW; School of Health and Rehabilitation Sciences, 1974The University of Queensland, Brisbane, QLD, Australia., Costa N; School of Health and Rehabilitation Sciences, 1974The University of Queensland, Brisbane, QLD, Australia.; 4334The University of Sydney, Sydney, NSW, Australia., Patton MA; School of Health and Rehabilitation Sciences, 1974The University of Queensland, Brisbane, QLD, Australia., Evans K; 4334The University of Sydney, Sydney, NSW, Australia.; Healthia Limited, Brisbane, QLD, Australia., Walsh K; Persistent Pain Management Service, 157829Metro South Health, Brisbane, QLD, Australia., Lonergan K, Setchell J; School of Health and Rehabilitation Sciences, 1974The University of Queensland, Brisbane, QLD, Australia.

Publikováno v: Qualitative health research [Qual Health Res] 2022 May; Vol. 32 (6), pp. 902-915. Date of Electronic Publication: 2022 Mar 26.