Conte, Matilde Immacolata

Conte, Matilde Immacolata  

Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli  

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Titolo Data di pubblicazione Autore(i) File
Deletion of the Overlapping Genes G6pd and Nemo Causes Severe form of Incontinentia Pigmenti Associated to Nervous System Delayed Development and Learning Disability. 1-gen-2012 Conte, Mi; Raimo, S; Paciolla, M; Pescatore, A; Esposito, E; Giuseppina Miano, M; Fusco, F; Ursini, Mv
Deletion of the overlapping genes G6PD and NEMO causes severe form of incontinentia pigmenti associated to nervous system delayed development and learning disabilities. 1-gen-2012 Conte MI; Raimo S; Paciolla M; Pescatore A; Esposito E; Miano MG; Fusco F; Ursini MV
A rare deletion of IKBKG promoter B in incontinentia pigmenti patient reveals the role of IKBKG promoter A during embryonic development. 1-gen-2011 Fusco, F; Pescatore, A; Conte, Mi; Paciolla, M; Lioi, Mb; Miano, Mg; Ursini, Mv
Gene Conversion at the Xq28 and novel non-recurrent deletions involving IKBKG/ NEMO and G6PD denote genomic instability causing incontinentia pigmenti. 1-gen-2011 Fusco, F; Paciolla, M; Conte, Mi; Pescatore, A; Lioi, Mb; Miano, Mg; Ursini, Mv