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Annelore Willaert

Showing results (1-10 of 5) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 24, 2021
Prevalence of Otological Disease in Turner Syndrome: A Systematic ReviewAlexander Geerardyn, Annelore Willaert, Brigitte Decallonne, et al.
International Journal of Pediatric Otorhinolaryngology|January 27, 2016
Congenital sternoclavicular dermoid sinusAnnelore Willaert, Liesje Bruninx, Greet Hens, et al.
American Journal of Medical Genetics. Part A|January 13, 2019
Vestibular dysfunction is a manifestation of 22q11.2 deletion syndromeAnnelore Willaert, Charlotte Van Eynde, Nicolas Verhaert, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndromeElke Loos, Nicolas Verhaert, Annelore Willaert, et al.
BMC Biology|March 17, 2022
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programmeMorag A Lewis, Neil J Ingham, Jing Chen, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 24, 2021
Prevalence of Otological Disease in Turner Syndrome: A Systematic ReviewAlexander Geerardyn, Annelore Willaert, Brigitte Decallonne, et al.
International Journal of Pediatric Otorhinolaryngology|January 27, 2016
Congenital sternoclavicular dermoid sinusAnnelore Willaert, Liesje Bruninx, Greet Hens, et al.
American Journal of Medical Genetics. Part A|January 13, 2019
Vestibular dysfunction is a manifestation of 22q11.2 deletion syndromeAnnelore Willaert, Charlotte Van Eynde, Nicolas Verhaert, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndromeElke Loos, Nicolas Verhaert, Annelore Willaert, et al.
BMC Biology|March 17, 2022
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programmeMorag A Lewis, Neil J Ingham, Jing Chen, et al.
Pageof 1