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Beatriz C A Mendes

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

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Journal of Human Genetics|December 6, 2018
Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humansAlex Marcel Moreira Dias, Karina Lezirovitz, Fernanda Stávale Nicastro, et al.
Brazilian Journal of Otorhinolaryngology|March 27, 2010
Multiprofessional committee on auditory health: COMUSADoris Ruthy Lewis, Silvio Antonio Monteiro Marone, Beatriz C A Mendes, et al.
Frontiers in Genetics|November 5, 2024
Genetic heterogeneity in autosomal recessive hearing loss: a survey of Brazilian familiesLarissa Nascimento Antunes, Alex Marcel Moreira Dias, Beatriz Cetalle Schiavo, et al.
European Journal of Human Genetics : EJHG|May 6, 2021
Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing lossAndré S Bueno, Kelly Nunes, Alex M M Dias, et al.
Scientific Reports|June 9, 2018
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing lossVitor G L Dantas, Manmeet H Raval, Angela Ballesteros, et al.
Pageof 1

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

Sort By:
Pageof 1
Journal of Human Genetics|December 6, 2018
Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humansAlex Marcel Moreira Dias, Karina Lezirovitz, Fernanda Stávale Nicastro, et al.
Brazilian Journal of Otorhinolaryngology|March 27, 2010
Multiprofessional committee on auditory health: COMUSADoris Ruthy Lewis, Silvio Antonio Monteiro Marone, Beatriz C A Mendes, et al.
Frontiers in Genetics|November 5, 2024
Genetic heterogeneity in autosomal recessive hearing loss: a survey of Brazilian familiesLarissa Nascimento Antunes, Alex Marcel Moreira Dias, Beatriz Cetalle Schiavo, et al.
European Journal of Human Genetics : EJHG|May 6, 2021
Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing lossAndré S Bueno, Kelly Nunes, Alex M M Dias, et al.
Scientific Reports|June 9, 2018
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing lossVitor G L Dantas, Manmeet H Raval, Angela Ballesteros, et al.
Pageof 1