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Showing results (681-690 of 723) with videos related to

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Prenatal Diagnosis|November 14, 2012
What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?F Coron, T Rousseau, G Jondeau, et al.
American Journal of Human Genetics|December 1, 2014
MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissectionsMathieu Barbier, Marie-Sylvie Gross, Mélodie Aubart, et al.
Human Genetics|September 7, 2002
Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutationsBruno Moulard, Pierre Genton, Djamel Grid, et al.
Brain : a Journal of Neurology|March 22, 2006
Delineation of the motor disorder of Lesch-Nyhan diseaseH A Jinnah, Jasper E Visser, James C Harris, et al.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
European Heart Journal|May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trialOlivier Milleron, Florence Arnoult, Jacques Ropers, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Rheumatology and Therapy|September 16, 2021
Antirheumatic Drug Intake Influence on Occurrence of COVID-19 Infection in Ambulatory Patients with Immune-Mediated Inflammatory Diseases: A Cohort StudyDebellemanière Guillaume, Bouvet Magalie, Elahi Sina, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Pageof 73

Showing results (681-690 of 723) with videos related to

Sort By:
Pageof 73
Prenatal Diagnosis|November 14, 2012
What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?F Coron, T Rousseau, G Jondeau, et al.
American Journal of Human Genetics|December 1, 2014
MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissectionsMathieu Barbier, Marie-Sylvie Gross, Mélodie Aubart, et al.
Human Genetics|September 7, 2002
Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutationsBruno Moulard, Pierre Genton, Djamel Grid, et al.
Brain : a Journal of Neurology|March 22, 2006
Delineation of the motor disorder of Lesch-Nyhan diseaseH A Jinnah, Jasper E Visser, James C Harris, et al.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
European Heart Journal|May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trialOlivier Milleron, Florence Arnoult, Jacques Ropers, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Rheumatology and Therapy|September 16, 2021
Antirheumatic Drug Intake Influence on Occurrence of COVID-19 Infection in Ambulatory Patients with Immune-Mediated Inflammatory Diseases: A Cohort StudyDebellemanière Guillaume, Bouvet Magalie, Elahi Sina, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Pageof 73