Your browser doesn't support javascript.
loading
Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment.
Kaheel, Hazem; Breß, Andreas; Hassan, Mohamed A; Shah, Aftab Ali; Amin, Mutaz; Bakhit, Yousuf H Y; Kniper, Marlies.
Affiliation
  • Kaheel H; Universitäts-HNO-Klinik Tübingen, Tübingen, Germany.
  • Breß A; Universitäts-HNO-Klinik Tübingen, Tübingen, Germany.
  • Hassan MA; Universitäts-HNO-Klinik Tübingen, Tübingen, Germany.
  • Shah AA; Department of Bioinformatics, Africa City of Technology, Khartoum, Sudan.
  • Amin M; Faculty of Biotechnology, University of Malakand, Malakand, Pakistan.
  • Bakhit YHY; Department of Biochemistry, Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
  • Kniper M; Department of Basic Medical Sciences, Faculty of Dentistry, University of Khartoum, Khartoum, Sudan.
Genet Res Int ; 2017: 5836525, 2017.
Article in En | MEDLINE | ID: mdl-29362677
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Genet Res Int Year: 2017 Document type: Article Affiliation country: Germany Country of publication: Egypt
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Genet Res Int Year: 2017 Document type: Article Affiliation country: Germany Country of publication: Egypt