Familial bilateral abductor vocal cord paralysis
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference21 articles.
1. Airway obstruction due to vocal cord paralysis in infants with hydrocephalus and meningomyelocele;Bluestone;Ann. Otol.,1972
2. Familial recurrent laryngeal nerve paralysis, a genetically fixed syndrome -additional remark on linkage of deficiency gene and HLA;Brunner;Laryngol. Rhinol. Otol.,1982
3. A review of laryngeal paralysis in dogs;Burbidge;Br. Vet. J.,1995
4. Familial vocal cord dysfunction;Cunningham;Pediatrics,1985
5. Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31;Feit;Am. J. Hum. Genet.,1998
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3. JS-X syndrome: A multiple congenital malformation with vocal cord paralysis, ear deformity, hearing loss, shoulder musculature underdevelopment, and X-linked recessive inheritance;International Journal of Pediatric Otorhinolaryngology;2015-07
4. Familial congenital bilateral vocal fold paralysis: A novel gene translocation;International Journal of Pediatric Otorhinolaryngology;2015-03
5. Paralyzed neonatal larynx in adduction. Case series, systematic review and analysis;International Journal of Pediatric Otorhinolaryngology;2013-01
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