Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment / 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.. - In: EUROPEAN JOURNAL OF HUMAN GENETICS. - ISSN 1018-4813. - (2011), pp. 102-107. [10.1038/ejhg.2010.142]

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

BRUNETTI PIERRI, NICOLA;
2011

2011
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment / 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.. - In: EUROPEAN JOURNAL OF HUMAN GENETICS. - ISSN 1018-4813. - (2011), pp. 102-107. [10.1038/ejhg.2010.142]
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/404417
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 110
  • ???jsp.display-item.citation.isi??? 100
social impact