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Hearing impairment in children with Stickler syndrome: review of phenotype and correlation with genotype

Frederic Acke (UGent) , Ingeborg Dhooge (UGent) and Els De Leenheer (UGent)
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Chicago
Acke, Frederic, Ingeborg Dhooge, and Els De Leenheer. 2012. “Hearing Impairment in Children with Stickler Syndrome: Review of Phenotype and Correlation with Genotype.” In European Society of Pediatric Otorhinolaryngology, 11th International Congress, Abstract Book, 108–108.
APA
Acke, F., Dhooge, I., & De Leenheer, E. (2012). Hearing impairment in children with Stickler syndrome: review of phenotype and correlation with genotype. European Society of Pediatric Otorhinolaryngology, 11th International congress, Abstract book (pp. 108–108). Presented at the 11th International congress of the European Society of Pediatric Otorhinolaryngology.
Vancouver
1.
Acke F, Dhooge I, De Leenheer E. Hearing impairment in children with Stickler syndrome: review of phenotype and correlation with genotype. European Society of Pediatric Otorhinolaryngology, 11th International congress, Abstract book. 2012. p. 108–108.
MLA
Acke, Frederic, Ingeborg Dhooge, and Els De Leenheer. “Hearing Impairment in Children with Stickler Syndrome: Review of Phenotype and Correlation with Genotype.” European Society of Pediatric Otorhinolaryngology, 11th International Congress, Abstract Book. 2012. 108–108. Print.
@inproceedings{2133676,
  articleno    = {abstract O098},
  author       = {Acke, Frederic and Dhooge, Ingeborg and De Leenheer, Els},
  booktitle    = {European Society of Pediatric Otorhinolaryngology, 11th International congress, Abstract book},
  language     = {eng},
  location     = {Amsterdam, The Netherlands},
  pages        = {abstract O098:108--abstract O098:108},
  title        = {Hearing impairment in children with Stickler syndrome: review of phenotype and correlation with genotype},
  year         = {2012},
}