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Acta Oto-Laryngologica Volume 115, 1995 - Issue 2
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Original

Physiopathological Investigations in a Family with a History of Unilateral Mereditary Deafness

G. Lina-Granade Laboratoire de Physiologic Sensorielle. URA CNRS 1447, Universiteé Claude Bernard, and Département d'ORL, Hôpital E. Herriot, Lyon, France
,
L. Collet Laboratoire de Physiologic Sensorielle. URA CNRS 1447, Universiteé Claude Bernard, and Département d'ORL, Hôpital E. Herriot, Lyon, France
&
A. Morgon Laboratoire de Physiologic Sensorielle. URA CNRS 1447, Universiteé Claude Bernard, and Département d'ORL, Hôpital E. Herriot, Lyon, France
Pages 196-201 | Published online: 30 Nov 2010

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. (2016) Guidelines for aetiological investigation into unilateral permanent childhood hearing impairment. Hearing, Balance and Communication 14:3, pages 146-155.
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Articles from other publishers (2)

Laurence Jonard, Magali Niasme-Grare, Crystel Bonnet, Delphine Feldmann, Isabelle Rouillon, Natalie Loundon, Catherine Calais, Hélène Catros, Albert David, Hélène Dollfus, Valérie Drouin-Garraud, Françoise Duriez, Marie Madeleine Eliot, Florence Fellmann, Christine Francannet, Brigitte Gilbert-Dussardier, Catherine Gohler, Cyril Goizet, Hubert Journel, Thierry Mom, Marie-Françoise Thuillier-Obstoy, Remy Couderc, Eréa Noël Garabédian, Françoise Denoyelle & Sandrine Marlin. (2010) Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct. International Journal of Pediatric Otorhinolaryngology 74:9, pages 1049-1053.
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Frederik G. Dikkers, Joke B. G. M. Verheij & Monique van Mechelen. (2016) Hereditary Congenital Unilateral Deafness: A New Disorder?. Annals of Otology, Rhinology & Laryngology 114:4, pages 332-337.
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