دورية أكاديمية
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.
العنوان: | Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment. |
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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 |
DOI: | 10.1038/ejhg.2010.142 |
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