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Reinhard Ramsebner

Showing results (11-20 of 17) with videos related to

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Ear and Hearing|May 9, 2007
High incidence of GJB2 mutations during screening of newborns for hearing loss in AustriaReinhard Ramsebner, Romana Volker, Trevor Lucas, et al.
The Laryngoscope|March 4, 2005
GJB2 mutations in hearing impairment: identification of a broad clinical spectrum for improved genetic counselingKlemens Frei, Reinhard Ramsebner, Trevor Lucas, et al.
Acta Oto-Laryngologica|November 10, 2016
The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in AustriaThomas Parzefall, Trevor Lucas, Martin Koenighofer, et al.
Audiology & Neuro-Otology|December 17, 2003
A novel connexin 26 mutation associated with autosomal recessive sensorineural deafnessKlemens Frei, Trevor Lucas, Reinhard Ramsebner, et al.
The Laryngoscope|December 2, 2009
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontiaReinhard Ramsebner, Martin Ludwig, Thomas Parzefall, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 4, 2013
Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter studyReinhard Ramsebner, Martin Ludwig, Trevor Lucas, et al.
European Journal of Human Genetics : EJHG|July 11, 2002
Connexin 26 mutations in cases of sensorineural deafness in eastern AustriaKlemens Frei, Károly Szuhai, Trevor Lucas, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Ear and Hearing|May 9, 2007
High incidence of GJB2 mutations during screening of newborns for hearing loss in AustriaReinhard Ramsebner, Romana Volker, Trevor Lucas, et al.
The Laryngoscope|March 4, 2005
GJB2 mutations in hearing impairment: identification of a broad clinical spectrum for improved genetic counselingKlemens Frei, Reinhard Ramsebner, Trevor Lucas, et al.
Acta Oto-Laryngologica|November 10, 2016
The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in AustriaThomas Parzefall, Trevor Lucas, Martin Koenighofer, et al.
Audiology & Neuro-Otology|December 17, 2003
A novel connexin 26 mutation associated with autosomal recessive sensorineural deafnessKlemens Frei, Trevor Lucas, Reinhard Ramsebner, et al.
The Laryngoscope|December 2, 2009
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontiaReinhard Ramsebner, Martin Ludwig, Thomas Parzefall, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 4, 2013
Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter studyReinhard Ramsebner, Martin Ludwig, Trevor Lucas, et al.
European Journal of Human Genetics : EJHG|July 11, 2002
Connexin 26 mutations in cases of sensorineural deafness in eastern AustriaKlemens Frei, Károly Szuhai, Trevor Lucas, et al.
Pageof 2