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Stanislas Lyonnet

Showing results (11-20 of 260) with videos related to

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Human Molecular Genetics|September 11, 2004
Polyalanine expansions in humanJeanne Amiel, Delphine Trochet, Mathieu Clément-Ziza, et al.
RNA (New York, N.Y.)|October 24, 2008
Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutionsMathieu Clément-Ziza, Arnold Munnich, Stanislas Lyonnet, et al.
Biotechniques|August 25, 2005
GeneRetriever: software to extract all genes and transcripts in between two genetic markers to assist design of human custom microarraysMathieu Clément-Ziza, Yehuda Brody, Arnold Munnich, et al.
Journal of Hepatology|February 23, 2008
miR-122, a paradigm for the role of microRNAs in the liverMuriel Girard, Emmanuel Jacquemin, Arnold Munnich, et al.
BMC Oral Health|June 22, 2023
Determinants of dental care use in patients with rare diseases: a qualitative explorationLisa Friedlander, Ariane Berdal, Valérie Cormier-Daire, et al.
American Journal of Medical Genetics. Part A|April 16, 2005
Adams-Oliver syndrome and hepatoportal sclerosis: occasional association or common mechanism?Muriel Girard, Jeanne Amiel, Monique Fabre, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 31, 2005
Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasisBogdan Hermeziu, Damien Sanlaville, Muriel Girard, et al.
Clinical Dysmorphology|December 5, 2012
Sporadic NF1 mutation associated with a de-novo 20q11.3 deletion explains the association of unusual facies, Moyamoya vasculopathy, and developmental delay, reported by Bertoli et al. in 2009Claudia Santoro, Valérie Malan, Marta Bertoli, et al.
Orphanet Journal of Rare Diseases|August 20, 2022
Consideration of oral health in rare disease expertise centres: a retrospective study on 39 rare diseases using text mining extraction methodLisa Friedlander, Marc Vincent, Ariane Berdal, et al.
Pediatric Pulmonology|August 31, 2004
PHOX2B gene mutation in a patient with late-onset central hypoventilationHa Trang, Béatrice Laudier, Delphine Trochet, et al.
Pageof 26

Showing results (11-20 of 260) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|September 11, 2004
Polyalanine expansions in humanJeanne Amiel, Delphine Trochet, Mathieu Clément-Ziza, et al.
RNA (New York, N.Y.)|October 24, 2008
Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutionsMathieu Clément-Ziza, Arnold Munnich, Stanislas Lyonnet, et al.
Biotechniques|August 25, 2005
GeneRetriever: software to extract all genes and transcripts in between two genetic markers to assist design of human custom microarraysMathieu Clément-Ziza, Yehuda Brody, Arnold Munnich, et al.
Journal of Hepatology|February 23, 2008
miR-122, a paradigm for the role of microRNAs in the liverMuriel Girard, Emmanuel Jacquemin, Arnold Munnich, et al.
BMC Oral Health|June 22, 2023
Determinants of dental care use in patients with rare diseases: a qualitative explorationLisa Friedlander, Ariane Berdal, Valérie Cormier-Daire, et al.
American Journal of Medical Genetics. Part A|April 16, 2005
Adams-Oliver syndrome and hepatoportal sclerosis: occasional association or common mechanism?Muriel Girard, Jeanne Amiel, Monique Fabre, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 31, 2005
Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasisBogdan Hermeziu, Damien Sanlaville, Muriel Girard, et al.
Clinical Dysmorphology|December 5, 2012
Sporadic NF1 mutation associated with a de-novo 20q11.3 deletion explains the association of unusual facies, Moyamoya vasculopathy, and developmental delay, reported by Bertoli et al. in 2009Claudia Santoro, Valérie Malan, Marta Bertoli, et al.
Orphanet Journal of Rare Diseases|August 20, 2022
Consideration of oral health in rare disease expertise centres: a retrospective study on 39 rare diseases using text mining extraction methodLisa Friedlander, Marc Vincent, Ariane Berdal, et al.
Pediatric Pulmonology|August 31, 2004
PHOX2B gene mutation in a patient with late-onset central hypoventilationHa Trang, Béatrice Laudier, Delphine Trochet, et al.
Pageof 26