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 variants / Morgan, A; Lenarduzzi, S; Cappellani, S; Pecile, V; Morgutti, M; Orzan, E; Ghiselli, S; Ambrosetti, U; Brumat, M; Gajendrarao, P; La Bianca, M; Faletra, F; Grosso, E; Sirchia, F; Sensi, A; Graziano, C; Seri, M; Gasparini, P; Girotto, G. - In: FRONTIERS IN GENETICS. - ISSN 1664-8021. - (2018). [10.3389/fgene.2018.0068]

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 variants

Ghiselli S;
2018-01-01

2018
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 variants / Morgan, A; Lenarduzzi, S; Cappellani, S; Pecile, V; Morgutti, M; Orzan, E; Ghiselli, S; Ambrosetti, U; Brumat, M; Gajendrarao, P; La Bianca, M; Faletra, F; Grosso, E; Sirchia, F; Sensi, A; Graziano, C; Seri, M; Gasparini, P; Girotto, G. - In: FRONTIERS IN GENETICS. - ISSN 1664-8021. - (2018). [10.3389/fgene.2018.0068]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/3044259
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