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A novel X-linked disorder with developmental delay and autistic features.
Kaya, Namik; Colak, Dilek; Albakheet, Albandary; Al-Owain, Mohammad; Abu-Dheim, Nada; Al-Younes, Banan; Al-Zahrani, Jawaher; Mukaddes, Nahit M; Dervent, Aysin; Al-Dosari, Naji; Al-Odaib, Ali; Kayaalp, Inci V; Al-Sayed, Moeenaladin; Al-Hassnan, Zuhair; Nester, Michael J; Al-Dosari, Mohammad; Al-Dhalaan, Hesham; Chedrawi, Aziza; Gunoz, Hulya; Karakas, Bedri; Sakati, Nadia; Alkuraya, Fowzan S; Gascon, Generaso G; Ozand, Pinar T.
Affiliation
  • Kaya N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. nkaya@kfshrc.edu.sa
Ann Neurol ; 71(4): 498-508, 2012 Apr.
Article in En | MEDLINE | ID: mdl-22213401
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / Child Development Disorders, Pervasive / Chromosomes, Human, X / Genetic Diseases, X-Linked Type of study: Prognostic_studies Limits: Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Ann Neurol Year: 2012 Type: Article Affiliation country: Saudi Arabia
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / Child Development Disorders, Pervasive / Chromosomes, Human, X / Genetic Diseases, X-Linked Type of study: Prognostic_studies Limits: Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Ann Neurol Year: 2012 Type: Article Affiliation country: Saudi Arabia