Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Trevor Lucas

Showing results (21-30 of 53) with videos related to

Pageof 6
Sort By:
Hearing Research|October 7, 2004
Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern AustriaKlemens Frei, Reinhard Ramsebner, Trevor Lucas, et al.
Dental Materials : Official Publication of the Academy of Dental Materials|August 11, 2007
Cytotoxicity of resin composites as a function of interface areaAlexander Franz, Franz König, Astrid Skolka, et al.
European Journal of Human Genetics : EJHG|September 28, 2006
Vasoactive intestinal peptide gene alterations in patients with idiopathic pulmonary arterial hypertensionInes Haberl, Klemens Frei, Reinhard Ramsebner, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 21, 2007
Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Dental Materials : Official Publication of the Academy of Dental Materials|October 14, 2008
Cytotoxicity of four categories of dental cementsMartina Schmid-Schwap, Alexander Franz, Franz König, et al.
Wiener Klinische Wochenschrift|July 23, 2017
Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing lossThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Clinical and Experimental Otorhinolaryngology|June 22, 2019
Spectrum of Novel Hereditary Hemorrhagic Telangiectasia Variants in an Austrian Patient CohortMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 24, 2007
Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|April 14, 2021
Incomplete penetrance of a novel SDHD variation causing familial head and neck paragangliomaMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Audiology & Neuro-Otology|May 8, 2014
A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie diseaseThomas Parzefall, Trevor Lucas, Markus Ritter, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Hearing Research|October 7, 2004
Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern AustriaKlemens Frei, Reinhard Ramsebner, Trevor Lucas, et al.
Dental Materials : Official Publication of the Academy of Dental Materials|August 11, 2007
Cytotoxicity of resin composites as a function of interface areaAlexander Franz, Franz König, Astrid Skolka, et al.
European Journal of Human Genetics : EJHG|September 28, 2006
Vasoactive intestinal peptide gene alterations in patients with idiopathic pulmonary arterial hypertensionInes Haberl, Klemens Frei, Reinhard Ramsebner, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 21, 2007
Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Dental Materials : Official Publication of the Academy of Dental Materials|October 14, 2008
Cytotoxicity of four categories of dental cementsMartina Schmid-Schwap, Alexander Franz, Franz König, et al.
Wiener Klinische Wochenschrift|July 23, 2017
Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing lossThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Clinical and Experimental Otorhinolaryngology|June 22, 2019
Spectrum of Novel Hereditary Hemorrhagic Telangiectasia Variants in an Austrian Patient CohortMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 24, 2007
Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in AustriaReinhard Ramsebner, Trevor Lucas, Christian Schoefer, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|April 14, 2021
Incomplete penetrance of a novel SDHD variation causing familial head and neck paragangliomaMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Audiology & Neuro-Otology|May 8, 2014
A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie diseaseThomas Parzefall, Trevor Lucas, Markus Ritter, et al.
Pageof 6