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Stanislas Lyonnet

Showing results (1-10 of 260) with videos related to

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Medecine Sciences : M/S|April 24, 2023
[Genome and genomic data: in between science and care]Stanislas Lyonnet
Nature Genetics|December 28, 2013
Enhancer mutations and phenotype modularityChristopher T Gordon, Stanislas Lyonnet
Advances in Experimental Medicine and Biology|November 2, 2006
Molecular bases of human neurocristopathiesHeather C Etchevers, Jeanne Amiel, Stanislas Lyonnet
Behavior Genetics|February 14, 2006
Academic impairment is the most frequent complication of neurofibromatosis type-1 (NF1) in childrenFrançois X Coudé, Claire Mignot, Stanislas Lyonnet, et al.
Laterality|January 18, 2006
Discontinuity in the fall of left-handedness in a French population: a May '68 effect?François X Coudé, Claire Mignot, Stanislas Lyonnet, et al.
Annals of the New York Academy of Sciences|December 24, 2010
Disruption of long-distance highly conserved noncoding elements in neurocristopathiesJeanne Amiel, Sabina Benko, Christopher T Gordon, et al.
Biologie Aujourd'Hui|August 12, 2011
[Cis-ruptions of highly conserved non-coding genomic elements distant from the SOX9 gene in the Pierre Robin sequence]Sabina Benko, Christopher T Gordon, Jeanne Amiel, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 19, 2011
Genetic factors in isolated and syndromic esophageal atresiaDavid Geneviève, Loïc de Pontual, Jeanne Amiel, et al.
Journal of Attention Disorders|May 15, 2007
Early grade repetition and inattention associated with neurofibromatosis type 1François X Coudé, Claire Mignot, Stanislas Lyonnet, et al.
Clinical Dysmorphology|December 6, 2008
Sporadic case of unusual facies, cerebral vascular anomalies and developmental delayMarta Bertoli, Nathalie Boddaert, Odile Raoul, et al.
Pageof 26

Showing results (1-10 of 260) with videos related to

Sort By:
Pageof 26
Medecine Sciences : M/S|April 24, 2023
[Genome and genomic data: in between science and care]Stanislas Lyonnet
Nature Genetics|December 28, 2013
Enhancer mutations and phenotype modularityChristopher T Gordon, Stanislas Lyonnet
Advances in Experimental Medicine and Biology|November 2, 2006
Molecular bases of human neurocristopathiesHeather C Etchevers, Jeanne Amiel, Stanislas Lyonnet
Behavior Genetics|February 14, 2006
Academic impairment is the most frequent complication of neurofibromatosis type-1 (NF1) in childrenFrançois X Coudé, Claire Mignot, Stanislas Lyonnet, et al.
Laterality|January 18, 2006
Discontinuity in the fall of left-handedness in a French population: a May '68 effect?François X Coudé, Claire Mignot, Stanislas Lyonnet, et al.
Annals of the New York Academy of Sciences|December 24, 2010
Disruption of long-distance highly conserved noncoding elements in neurocristopathiesJeanne Amiel, Sabina Benko, Christopher T Gordon, et al.
Biologie Aujourd'Hui|August 12, 2011
[Cis-ruptions of highly conserved non-coding genomic elements distant from the SOX9 gene in the Pierre Robin sequence]Sabina Benko, Christopher T Gordon, Jeanne Amiel, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 19, 2011
Genetic factors in isolated and syndromic esophageal atresiaDavid Geneviève, Loïc de Pontual, Jeanne Amiel, et al.
Journal of Attention Disorders|May 15, 2007
Early grade repetition and inattention associated with neurofibromatosis type 1François X Coudé, Claire Mignot, Stanislas Lyonnet, et al.
Clinical Dysmorphology|December 6, 2008
Sporadic case of unusual facies, cerebral vascular anomalies and developmental delayMarta Bertoli, Nathalie Boddaert, Odile Raoul, et al.
Pageof 26