Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations.

Anna Morgan, Stefania Lenarduzzi, Stefania Cappellani, Vanna Pecile, Marcello Morgutti, Eva Orzan, Sara Ghiselli, Umberto Ambrosetti, Marco Brumat, Poornima Gajendrarao, Martina La Bianca, Flavio Faletra, E. Grosso, Fabio Sirchia, Alberto Sensi, C. Graziano, M Seri, Paolo Gasparini, Giorgia Girotto

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)681
JournalFrontiers in Genetics
Volume2018 Dec 21
Issue number9:681
Publication statusPublished - 2018

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