دورية أكاديمية

Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.

التفاصيل البيبلوغرافية
العنوان: Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.
المؤلفون: BRUNETTI PIERRI, NICOLA, Paciorkowski AR, Ciccone R, Mina ED, Bonaglia MC, Borgatti R, Schaaf CP, Sutton VR, Xia Z, Jelluma N, Ruivenkamp C, Bertrand M, de Ravel TJ, Jayakar P, Belli S, Rocchetti K, Pantaleoni C, D'Arrigo S, Hughes J, Cheung SW, Zuffardi O, Stankiewicz P.
المساهمون: BRUNETTI PIERRI, Nicola, Paciorkowski, Ar, Ciccone, R, Mina, Ed, Bonaglia, Mc, Borgatti, R, Schaaf, Cp, Sutton, Vr, Xia, Z, Jelluma, N, Ruivenkamp, C, Bertrand, M, de Ravel, Tj, Jayakar, P, Belli, S, Rocchetti, K, Pantaleoni, C, D'Arrigo, S, Hughes, J, Cheung, Sw, Zuffardi, O, Stankiewicz, P.
سنة النشر: 2011
المجموعة: IRIS Università degli Studi di Napoli Federico II
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000285139600017; firstpage:102; lastpage:107; journal:EUROPEAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11588/404417Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-78650067986
DOI: 10.1038/ejhg.2010.142
الإتاحة: https://doi.org/10.1038/ejhg.2010.142Test
http://hdl.handle.net/11588/404417Test
رقم الانضمام: edsbas.9C0DB7EF
قاعدة البيانات: BASE