Genetics of Inner Ear Malformations: A Review

Autor: Renzo Manara, Roberta Cenedese, Flavia Sorrentino, Davide Brotto, Roberto Bovo, Irene Avato, Patrizia Trevisi

Publikováno v: Audiology Research
Audiology Research, Vol 11, Iss 47, Pp 524-536 (2021)

Inner ear malformations are present in 20% of patients with sensorineural hearing loss. Although the first descriptions date to the 18th century, in recent years the knowledge about these conditions has experienced terrific improvement. Currently, mo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c43df7a3a264330834bd11726fb71a8
http://europepmc.org/articles/PMC8544219

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Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss.

Autor: Lallar M; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India., Arora V; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India., Saxena R; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India., Puri RD; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India., Verma IC; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.

Publikováno v: Journal of pediatric genetics [J Pediatr Genet] 2021 Mar; Vol. 10 (1), pp. 70-73. Date of Electronic Publication: 2020 Mar 09.