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S Jacquemont

Showing results (1-10 of 28) with videos related to

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Annales De Dermatologie Et De Venereologie|October 11, 2007
[NF1: Molecular testing in clinical practice]C Rieubland, D Vidaud, S Jacquemont
Best Practice & Research. Clinical Endocrinology & Metabolism|April 14, 2012
Genetic testing in patients with obesityF Phan-Hug, J S Beckmann, S Jacquemont
American Journal of Medical Genetics|August 18, 2000
Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's reportS Jacquemont, S Barbarot, M Bocéno, et al.
Pediatrics and Neonatology|June 20, 2013
Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital MalformationsM Broome, Y Vial, S Jacquemont, et al.
Neuroepidemiology|February 24, 2006
Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.
Digestive Diseases and Sciences|July 4, 1998
Rapid diagnostic test for detection of Cys282Tyr mutation in hereditary hemochromatosisM T Andre, S Jacquemont, S Renault, et al.
Bioinformatics (Oxford, England)|July 13, 2016
New quality measure for SNP array based CNV detectionA Macé, M A Tuke, J S Beckmann, et al.
American Journal of Medical Genetics. Part A|May 13, 2008
Autosomal dominant spondylocarpotarsal synostosis syndrome: phenotypic homogeneity and genetic heterogeneityB Isidor, V Cormier-Daire, M Le Merrer, et al.
Journal of Medical Genetics|February 4, 2005
Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformationsC Le Caignec, M Boceno, P Saugier-Veber, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2007
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA)E M Pitchon, F Cachat, S Jacquemont, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Annales De Dermatologie Et De Venereologie|October 11, 2007
[NF1: Molecular testing in clinical practice]C Rieubland, D Vidaud, S Jacquemont
Best Practice & Research. Clinical Endocrinology & Metabolism|April 14, 2012
Genetic testing in patients with obesityF Phan-Hug, J S Beckmann, S Jacquemont
American Journal of Medical Genetics|August 18, 2000
Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's reportS Jacquemont, S Barbarot, M Bocéno, et al.
Pediatrics and Neonatology|June 20, 2013
Complete Maxillo-Mandibular Syngnathia in a Newborn with Multiple Congenital MalformationsM Broome, Y Vial, S Jacquemont, et al.
Neuroepidemiology|February 24, 2006
Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.
Digestive Diseases and Sciences|July 4, 1998
Rapid diagnostic test for detection of Cys282Tyr mutation in hereditary hemochromatosisM T Andre, S Jacquemont, S Renault, et al.
Bioinformatics (Oxford, England)|July 13, 2016
New quality measure for SNP array based CNV detectionA Macé, M A Tuke, J S Beckmann, et al.
American Journal of Medical Genetics. Part A|May 13, 2008
Autosomal dominant spondylocarpotarsal synostosis syndrome: phenotypic homogeneity and genetic heterogeneityB Isidor, V Cormier-Daire, M Le Merrer, et al.
Journal of Medical Genetics|February 4, 2005
Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformationsC Le Caignec, M Boceno, P Saugier-Veber, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2007
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA)E M Pitchon, F Cachat, S Jacquemont, et al.
Pageof 3