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Sandrine Marlin

Showing results (11-20 of 117) 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|July 26, 2017
Noonan Syndrome: An Underestimated Cause of Severe to Profound Sensorineural Hearing Impairment. Which Clues to Suspect the Diagnosis?Alban Ziegler, Natalie Loundon, Laurence Jonard, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2012
Cochlear implantation and congenital deafness: perceptive and lexical results in 2 genetically pediatric identified populationWissame El Bakkouri, Natalie Loundon, Briac Thierry, et al.
Stem Cell Research|March 29, 2023
Two induced pluripotent stem cell (iPSC) lines derived from patients affected by Waardenburg syndrome type 1 retain potential to activate neural crest markersMansour Alkobtawi, Patrick Pla, Brigitte Onteniente, et al.
Plos One|August 1, 2012
Screening of MITF and SOX10 regulatory regions in Waardenburg syndrome type 2Viviane Baral, Asma Chaoui, Yuli Watanabe, et al.
Disability and Rehabilitation|April 13, 2019
Psychosocial determinants associated with quality of life in people with usher syndrome. A scoping reviewMarine Arcous, Olivier Putois, Sophie Dalle-Nazébi, et al.
Muscle & Nerve|April 12, 2011
Facial, lingual, and pharyngeal electromyography in infants with Pierre Robin sequenceFrancis Renault, Jean-Jacques Baudon, Eva Galliani, et al.
European Journal of Medical Genetics|September 20, 2019
MED12 missense mutation in a three-generation family. Clinical characterization of MED12-related disorders and literature reviewElisa Rubinato, Sophie Rondeau, Fabienne Giuliano, et al.
Molecular Genetics & Genomic Medicine|August 2, 2020
Functional and genetic analyses of ZYG11B provide evidences for its involvement in OAVSAngèle Tingaud-Sequeira, Aurélien Trimouille, Sandrine Marlin, et al.
European Journal of Medical Genetics|June 26, 2026
Hearing outcomes after cochlear implantation in two patients with ATP6V1B2-related deafness and onychodystrophySarah Chamieh, Pauline Marzin, Sophie Achard, et al.
European Journal of Medical Genetics|February 28, 2016
A case of mild CHARGE syndrome associated with a splice site mutation in CHD7Constance Wells, Natalie Loundon, Noël Garabedian, et al.
Pageof 12

Showing results (11-20 of 117) with videos related to

Sort By:
Pageof 12
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 26, 2017
Noonan Syndrome: An Underestimated Cause of Severe to Profound Sensorineural Hearing Impairment. Which Clues to Suspect the Diagnosis?Alban Ziegler, Natalie Loundon, Laurence Jonard, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2012
Cochlear implantation and congenital deafness: perceptive and lexical results in 2 genetically pediatric identified populationWissame El Bakkouri, Natalie Loundon, Briac Thierry, et al.
Stem Cell Research|March 29, 2023
Two induced pluripotent stem cell (iPSC) lines derived from patients affected by Waardenburg syndrome type 1 retain potential to activate neural crest markersMansour Alkobtawi, Patrick Pla, Brigitte Onteniente, et al.
Plos One|August 1, 2012
Screening of MITF and SOX10 regulatory regions in Waardenburg syndrome type 2Viviane Baral, Asma Chaoui, Yuli Watanabe, et al.
Disability and Rehabilitation|April 13, 2019
Psychosocial determinants associated with quality of life in people with usher syndrome. A scoping reviewMarine Arcous, Olivier Putois, Sophie Dalle-Nazébi, et al.
Muscle & Nerve|April 12, 2011
Facial, lingual, and pharyngeal electromyography in infants with Pierre Robin sequenceFrancis Renault, Jean-Jacques Baudon, Eva Galliani, et al.
European Journal of Medical Genetics|September 20, 2019
MED12 missense mutation in a three-generation family. Clinical characterization of MED12-related disorders and literature reviewElisa Rubinato, Sophie Rondeau, Fabienne Giuliano, et al.
Molecular Genetics & Genomic Medicine|August 2, 2020
Functional and genetic analyses of ZYG11B provide evidences for its involvement in OAVSAngèle Tingaud-Sequeira, Aurélien Trimouille, Sandrine Marlin, et al.
European Journal of Medical Genetics|June 26, 2026
Hearing outcomes after cochlear implantation in two patients with ATP6V1B2-related deafness and onychodystrophySarah Chamieh, Pauline Marzin, Sophie Achard, et al.
European Journal of Medical Genetics|February 28, 2016
A case of mild CHARGE syndrome associated with a splice site mutation in CHD7Constance Wells, Natalie Loundon, Noël Garabedian, et al.
Pageof 12