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 journalArticle

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

Cite this

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

In: Frontiers in Genetics, Vol. 2018 Dec 21, No. 9:681, 2018, p. 681.

Research output: Contribution to journalArticle

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AU - Morgan, Anna

AU - Lenarduzzi, Stefania

AU - Cappellani, Stefania

AU - Pecile, Vanna

AU - Morgutti, Marcello

AU - Orzan, Eva

AU - Ghiselli, Sara

AU - Ambrosetti, Umberto

AU - Brumat, Marco

AU - Gajendrarao, Poornima

AU - Bianca, Martina La

AU - Faletra, Flavio

AU - Grosso, E.

AU - Sirchia, Fabio

AU - Sensi, Alberto

AU - Graziano, C.

AU - Seri, M

AU - Gasparini, Paolo

AU - Girotto, Giorgia

PY - 2018

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U2 - 10.3389/fgene.2018.00681

DO - 10.3389/fgene.2018.00681

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VL - 2018 Dec 21

SP - 681

JO - Frontiers in Genetics

JF - Frontiers in Genetics

SN - 1664-8021

IS - 9:681

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