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Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches.
Granata, Paola; Cocciadiferro, Dario; Zito, Alessandra; Pessina, Chiara; Bassani, Alessandro; Zambonin, Fabio; Novelli, Antonio; Fasano, Mauro; Casalone, Rosario.
Affiliation
  • Granata P; Cytogenetics and Medical Genetics Unit, Department of Services, ASST dei Sette Laghi, Varese, Italy.
  • Cocciadiferro D; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Ospedale Pediatrico Bambino Gesù, Roma, Italy.
  • Zito A; Cytogenetics and Medical Genetics Unit, Department of Services, ASST dei Sette Laghi, Varese, Italy.
  • Pessina C; Department of Medicine and Surgery, University of Insubria, Varese, Italy.
  • Bassani A; Cytogenetics and Medical Genetics Unit, Department of Services, ASST dei Sette Laghi, Varese, Italy.
  • Zambonin F; Department of Medicine and Surgery, University of Insubria, Varese, Italy.
  • Novelli A; Cytogenetics and Medical Genetics Unit, Department of Services, ASST dei Sette Laghi, Varese, Italy.
  • Fasano M; Child Neuropsychiatry Unit, Department of Maternal and Child Health, ASST dei Sette Laghi, Varese, Italy.
  • Casalone R; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Ospedale Pediatrico Bambino Gesù, Roma, Italy.
Front Genet ; 13: 798607, 2022.
Article de En | MEDLINE | ID: mdl-35368691
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies / Risk_factors_studies Langue: En Journal: Front Genet Année: 2022 Type de document: Article Pays d'affiliation: Italie Pays de publication: Suisse
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies / Risk_factors_studies Langue: En Journal: Front Genet Année: 2022 Type de document: Article Pays d'affiliation: Italie Pays de publication: Suisse