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Page 1
Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.
Genes (Basel). 2021 Apr 13;12(4):566. doi: 10.3390/genes12040566.
Genes (Basel). 2021.
PMID: 33924653
Free PMC article.
The SLC26A4 c.706C>G (p.Leu236Val) Variant is a Frequent Cause of Hearing Impairment in Filipino Cochlear Implantees.
Chiong CM, Reyes-Quintos MRT, Yarza TKL, Tobias-Grasso CAM, Acharya A, Leal SM, Mohlke KL, Mayol NL, Cutiongco-de la Paz EM, Santos-Cortez RLP.
Chiong CM, et al. Among authors: tobias grasso cam.
Otol Neurotol. 2018 Sep;39(8):e726-e730. doi: 10.1097/MAO.0000000000001893.
Otol Neurotol. 2018.
PMID: 30113565
Free PMC article.
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Lack of Methylation Changes in GJB2 and RB1 Non-coding Regions of Cochlear Implant Patients with Sensorineural Hearing Loss.
Sumalde AAM, Yang IV, Yarza TKL, Tobias-Grasso CAM, Tantoco MLC, Davidson E, Chan AL, Azamian MS, Cruz TLG, Lalani SR, Reyes-Quintos MRT, Cutiongco-de la Paz EM, Santos-Cortez RLP, Chiong CM.
Sumalde AAM, et al. Among authors: tobias grasso cam.
Acta Med Philipp. 2023 Sep 28;57(9):116-120. doi: 10.47895/amp.v57i9.5200.
Acta Med Philipp. 2023.
PMID: 37990697
Free PMC article.
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