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Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders.
Gimelli, Stefania; Capra, Valeria; Di Rocco, Maja; Leoni, Massimiliano; Mirabelli-Badenier, Marisol; Schiaffino, Maria Cristina; Fiorio, Patrizia; Cuoco, Cristina; Gimelli, Giorgio; Tassano, Elisa.
Affiliation
  • Gimelli S; Service of Genetic Medicine, University Hospitals of Geneva, Geneva, Switzerland.
  • Capra V; U.O. Neurochirurgia, Istituto G.Gaslini, Genoa, Italy.
  • Di Rocco M; USD Malattie Rare, Istituto G Gaslini, Genoa, Italy.
  • Leoni M; Pediatria II, Istituto G Gaslini, Genoa, Italy.
  • Mirabelli-Badenier M; DINOMGI Dipartimento-Università di Genova; U.O. Neuropsichiatria infantile, Istituto G. Gaslini, Genoa, Italy.
  • Schiaffino MC; Dipartimento di Pediatria, Istituto G Gaslini, Genoa, Italy.
  • Fiorio P; Laboratorio di Citogenetica, Istituto G. Gaslini, G.Gaslini 5, Genoa, 16147, Italy.
  • Cuoco C; Laboratorio di Citogenetica, Istituto G. Gaslini, G.Gaslini 5, Genoa, 16147, Italy.
  • Gimelli G; Laboratorio di Citogenetica, Istituto G. Gaslini, G.Gaslini 5, Genoa, 16147, Italy.
  • Tassano E; Laboratorio di Citogenetica, Istituto G. Gaslini, G.Gaslini 5, Genoa, 16147, Italy.
Mol Cytogenet ; 7: 54, 2014.
Article in En | MEDLINE | ID: mdl-25478008
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Full text: 1 Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Mol Cytogenet Year: 2014 Type: Article Affiliation country: Switzerland
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Full text: 1 Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Mol Cytogenet Year: 2014 Type: Article Affiliation country: Switzerland