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Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability.
Ehtesham, Naeim; Mosallaei, Meysam; Beheshtian, Maryam; Khoshbakht, Shahrouz; Fadaee, Mahsa; Vazehan, Raheleh; Faraji Zonooz, Mehrshid; Karimzadeh, Parvaneh; Kahrizi, Kimia; Najmabadi, Hossein.
Affiliation
  • Ehtesham N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Mosallaei M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Beheshtian M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Khoshbakht S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Fadaee M; Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran.
  • Vazehan R; Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran.
  • Faraji Zonooz M; Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran.
  • Karimzadeh P; Department of Pediatric Neurology, School of Medicine, Pediatric Neurology Research Center, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Arch Iran Med ; 25(12): 788-797, 2022 12 01.
Article de En | MEDLINE | ID: mdl-37543906
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Déficience intellectuelle Type d'étude: Risk_factors_studies Limites: Child / Humans Pays/Région comme sujet: Asia Langue: En Journal: Arch Iran Med Année: 2022 Type de document: Article Pays d'affiliation: Iran Pays de publication: Iran
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Déficience intellectuelle Type d'étude: Risk_factors_studies Limites: Child / Humans Pays/Région comme sujet: Asia Langue: En Journal: Arch Iran Med Année: 2022 Type de document: Article Pays d'affiliation: Iran Pays de publication: Iran