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M Grati

Showing results (1-10 of 6) with videos related to

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Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNB9 and DFNB12S Yasunaga, M Grati, C Petit
Cell Death & Disease|March 11, 2016
Rescue from early-onset hearing loss in a mouse model lacking the cyclin-dependent kinase inhibitor p19Ink4dQ Ma, M Grati, F Bai, et al.
American Journal of Human Genetics|July 21, 2000
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9S Yasunaga, M Grati, S Chardenoux, et al.
Nature Genetics|April 7, 1999
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafnessS Yasunaga, M Grati, M Cohen-Salmon, et al.
American Journal of Medical Genetics|December 22, 1999
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutationS Masmoudi, I Charfedine, M Hmani, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNB9 and DFNB12S Yasunaga, M Grati, C Petit
Cell Death & Disease|March 11, 2016
Rescue from early-onset hearing loss in a mouse model lacking the cyclin-dependent kinase inhibitor p19Ink4dQ Ma, M Grati, F Bai, et al.
American Journal of Human Genetics|July 21, 2000
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9S Yasunaga, M Grati, S Chardenoux, et al.
Nature Genetics|April 7, 1999
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafnessS Yasunaga, M Grati, M Cohen-Salmon, et al.
American Journal of Medical Genetics|December 22, 1999
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutationS Masmoudi, I Charfedine, M Hmani, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Pageof 1