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Carlo Ceglia

Showing results (1-10 of 6) with videos related to

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Maritime Studies : MAST|March 20, 2025
Neither private nor new: unpacking narratives of 'ocean privatisation'Carlo Ceglia, Kimberley Peters, Philip Steinberg
Gene|December 4, 2013
Identification of a deletion in the NDUFS4 gene using array-comparative genomic hybridization in a patient with suspected mitochondrial respiratory diseaseBarbara Lombardo, Carlo Ceglia, Marina Tarsitano, et al.
The Clinical Journal of Pain|January 29, 2014
Molecular analysis of cluster headacheFederica Zarrilli, Rossella Tomaiuolo, Carlo Ceglia, et al.
Gene|December 10, 2013
Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowthMarina Tarsitano, Carlo Ceglia, Antonio Novelli, et al.
Molecular Cytogenetics|March 31, 2015
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing lossSandra Iossa, Valerio Costa, Virginia Corvino, et al.
Molecular Genetics & Genomic Medicine|December 19, 2019
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rateIlaria Catusi, Maria Paola Recalcati, Ilaria Bestetti, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Maritime Studies : MAST|March 20, 2025
Neither private nor new: unpacking narratives of 'ocean privatisation'Carlo Ceglia, Kimberley Peters, Philip Steinberg
Gene|December 4, 2013
Identification of a deletion in the NDUFS4 gene using array-comparative genomic hybridization in a patient with suspected mitochondrial respiratory diseaseBarbara Lombardo, Carlo Ceglia, Marina Tarsitano, et al.
The Clinical Journal of Pain|January 29, 2014
Molecular analysis of cluster headacheFederica Zarrilli, Rossella Tomaiuolo, Carlo Ceglia, et al.
Gene|December 10, 2013
Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowthMarina Tarsitano, Carlo Ceglia, Antonio Novelli, et al.
Molecular Cytogenetics|March 31, 2015
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing lossSandra Iossa, Valerio Costa, Virginia Corvino, et al.
Molecular Genetics & Genomic Medicine|December 19, 2019
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rateIlaria Catusi, Maria Paola Recalcati, Ilaria Bestetti, et al.
Pageof 1