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ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review.
Kamal, Neda; Khamirani, Hossein Jafari; Mohammadi, Sanaz; Dastgheib, Seyed Alireza; Dianatpour, Mehdi; Tabei, Seyed Mohammad Bagher.
Affiliation
  • Kamal N; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Khamirani HJ; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Mohammadi S; Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dastgheib SA; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dianatpour M; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran; Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Tabei SMB; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran; Maternal-fetal Medicine Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: Tabeismb@sums.ac.ir.
Eur J Med Genet ; 65(7): 104522, 2022 Jul.
Article de En | MEDLINE | ID: mdl-35618198
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Troubles du développement neurologique / Déficience intellectuelle Type d'étude: Etiology_studies / Prognostic_studies Limites: Humans / Male Pays/Région comme sujet: Asia Langue: En Journal: Eur J Med Genet Sujet du journal: GENETICA MEDICA Année: 2022 Type de document: Article Pays d'affiliation: 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: Troubles du développement neurologique / Déficience intellectuelle Type d'étude: Etiology_studies / Prognostic_studies Limites: Humans / Male Pays/Région comme sujet: Asia Langue: En Journal: Eur J Med Genet Sujet du journal: GENETICA MEDICA Année: 2022 Type de document: Article Pays d'affiliation: Iran