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Dominique Weil

Showing results (71-80 of 84) with videos related to

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Elife|December 20, 2019
GC content shapes mRNA storage and decay in human cellsMaïté Courel, Yves Clément, Clémentine Bossevain, et al.
BMC Medical Genetics|May 28, 2010
Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathyDa-Yong Wang, Yi-Chen Wang, Dominique Weil, et al.
Orphanet Journal of Rare Diseases|December 3, 2013
Characteristics and management of congenital esophageal stenosis: findings from a multicenter studyLaurent Michaud, Frédéric Coutenier, Guillaume Podevin, et al.
Plos One|June 14, 2014
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafnessZied Riahi, Crystel Bonnet, Rim Zainine, et al.
Molecular Cell|October 5, 2024
Cell-cycle-dependent mRNA localization in P-bodiesAdham Safieddine, Marie-Noëlle Benassy, Thomas Bonte, et al.
Journal of Pediatric Surgery|July 20, 2010
Wandering spleen in children: multicenter retrospective studyCaroline Fiquet-Francois, Mohamed Belouadah, Hugues Ludot, et al.
Nature Genetics|July 2, 2003
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31Philomena Mburu, Mirna Mustapha, Anabel Varela, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Journal of Medical Genetics|September 12, 2006
Development of a genotyping microarray for Usher syndromeFrans P M Cremers, William J Kimberling, Maigi Külm, et al.
Journal of Pediatric Surgery|August 13, 2013
Esophageal atresia: data from a national cohortRony Sfeir, Arnaud Bonnard, Naziha Khen-Dunlop, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Elife|December 20, 2019
GC content shapes mRNA storage and decay in human cellsMaïté Courel, Yves Clément, Clémentine Bossevain, et al.
BMC Medical Genetics|May 28, 2010
Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathyDa-Yong Wang, Yi-Chen Wang, Dominique Weil, et al.
Orphanet Journal of Rare Diseases|December 3, 2013
Characteristics and management of congenital esophageal stenosis: findings from a multicenter studyLaurent Michaud, Frédéric Coutenier, Guillaume Podevin, et al.
Plos One|June 14, 2014
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafnessZied Riahi, Crystel Bonnet, Rim Zainine, et al.
Molecular Cell|October 5, 2024
Cell-cycle-dependent mRNA localization in P-bodiesAdham Safieddine, Marie-Noëlle Benassy, Thomas Bonte, et al.
Journal of Pediatric Surgery|July 20, 2010
Wandering spleen in children: multicenter retrospective studyCaroline Fiquet-Francois, Mohamed Belouadah, Hugues Ludot, et al.
Nature Genetics|July 2, 2003
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31Philomena Mburu, Mirna Mustapha, Anabel Varela, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Journal of Medical Genetics|September 12, 2006
Development of a genotyping microarray for Usher syndromeFrans P M Cremers, William J Kimberling, Maigi Külm, et al.
Journal of Pediatric Surgery|August 13, 2013
Esophageal atresia: data from a national cohortRony Sfeir, Arnaud Bonnard, Naziha Khen-Dunlop, et al.
Pageof 9