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Showing results (81-90 of 223) with videos related to

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Human Molecular Genetics|December 1, 1995
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
Nature Genetics|April 1, 1996
XNP mutation in a large family with Juberg-Marsidi syndromeL Villard, J Gecz, J F Mattéi, et al.
Neuroimage|December 29, 2005
Parieto-occipital grey matter abnormalities in children with Williams syndromeN Boddaert, F Mochel, I Meresse, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, R Salomon, J Amiel, et al.
American Journal of Human Genetics|February 11, 1999
Both recessive and dominant forms of anhidrotic/hypohidrotic ectodermal dysplasia map to chromosome 2q11-q13L Baala, S Hadj Rabia, J Zlotogora, et al.
Annals of Neurology|October 12, 2000
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutationV Pingault, A Guiochon-Mantel, N Bondurand, et al.
American Journal of Medical Genetics|January 20, 1997
Microsatellite DNA markers detects 95% of chromosome 22q11 deletionsD Bonnet, V Cormier-Daire, J Kachaner, et al.
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.
The Journal of Clinical Investigation|August 1, 1994
Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophyB Fournier, J M Saudubray, B Benichou, et al.
Oncogene Research|July 1, 1987
Expression of c-myc is under dietary control in rat liverD Corcos, S Vaulont, N Denis, et al.
Pageof 23

Showing results (81-90 of 223) with videos related to

Sort By:
Pageof 23
Human Molecular Genetics|December 1, 1995
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
Nature Genetics|April 1, 1996
XNP mutation in a large family with Juberg-Marsidi syndromeL Villard, J Gecz, J F Mattéi, et al.
Neuroimage|December 29, 2005
Parieto-occipital grey matter abnormalities in children with Williams syndromeN Boddaert, F Mochel, I Meresse, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, R Salomon, J Amiel, et al.
American Journal of Human Genetics|February 11, 1999
Both recessive and dominant forms of anhidrotic/hypohidrotic ectodermal dysplasia map to chromosome 2q11-q13L Baala, S Hadj Rabia, J Zlotogora, et al.
Annals of Neurology|October 12, 2000
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutationV Pingault, A Guiochon-Mantel, N Bondurand, et al.
American Journal of Medical Genetics|January 20, 1997
Microsatellite DNA markers detects 95% of chromosome 22q11 deletionsD Bonnet, V Cormier-Daire, J Kachaner, et al.
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.
The Journal of Clinical Investigation|August 1, 1994
Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophyB Fournier, J M Saudubray, B Benichou, et al.
Oncogene Research|July 1, 1987
Expression of c-myc is under dietary control in rat liverD Corcos, S Vaulont, N Denis, et al.
Pageof 23