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2021 | 2 |
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Page 1
Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene.
Genes (Basel). 2021 Jul 6;12(7):1043. doi: 10.3390/genes12071043.
Genes (Basel). 2021.
PMID: 34356059
Free PMC article.
Combined exome and whole transcriptome sequencing identifies a de novo intronic SRCAP variant causing DEHMBA syndrome with severe sleep disorder.
Morlino S, Vaccaro L, Leone MP, Nardella G, Bisceglia L, Ortore RP, Verzicco G, Cassano L, Castori M, Cacchiarelli D, Micale L.
Morlino S, et al. Among authors: ortore rp.
J Hum Genet. 2024 Mar 7. doi: 10.1038/s10038-024-01240-x. Online ahead of print.
J Hum Genet. 2024.
PMID: 38448605
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Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family.
Ortore RP, Leone MP, Palumbo O, Petracca A, Trecca EMC, D'Ecclesia A, Vigliaroli CL, Micale L, Longo F, Melchionda S, Castori M.
Ortore RP, et al.
Audiol Res. 2021 Sep 9;11(3):443-451. doi: 10.3390/audiolres11030041.
Audiol Res. 2021.
PMID: 34562879
Free PMC article.
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Speech recognition with BAHA simulator in subjects with acquired unilateral sensorineural hearing loss.
Bovo R, Prosser S, Ortore RP, Martini A.
Bovo R, et al. Among authors: ortore rp.
Acta Otolaryngol. 2011 Jun;131(6):633-9. doi: 10.3109/00016489.2010.544675. Epub 2011 Jan 31.
Acta Otolaryngol. 2011.
PMID: 21281058
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