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S Lyonnet

Showing results (91-100 of 223) with videos related to

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L'Encephale|November 25, 2018
[Child psychiatry interventions in patients with 22q11 deletion syndrome: From treatment to prevention]A Novo, L Woestelandt, B Rousselot-Pailley, et al.
American Journal of Human Genetics|April 29, 1998
Mutations of the RET-GDNF signaling pathway in Ondine's curseJ Amiel, R Salomon, T Attié, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1996
[Isolated neonatal dysfunction of brainstem]V Abadie, G Chéron, S Lyonnet, et al.
Journal of Medical Genetics|July 31, 2001
B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?P Edery, F Le Deist, M L Briard, et al.
American Journal of Medical Genetics|January 30, 1995
Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?P Saugier-Veber, A Munnich, S Lyonnet, et al.
American Journal of Medical Genetics|October 15, 1994
Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindredE Dow, S Cross, D J Wolgemuth, et al.
Journal of Medical Genetics|March 10, 2001
MECP2 mutation in non-fatal, non-progressive encephalopathy in a maleB Imessaoudene, J P Bonnefont, G Royer, et al.
European Journal of Biochemistry|April 15, 1989
Apolipoprotein-E-gene expression in rat liver during development in relation to insulin and glucagonM Mangeney, P Cardot, S Lyonnet, et al.
American Journal of Medical Genetics|March 17, 1997
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeV Cormier-Daire, M Le Merrer, N Gigarel, et al.
Journal of Medical Genetics|February 12, 2002
Dysmorphism, variable overgrowth, normal bone age, and severe developmental delay: a "Sotos-like" syndrome?J Amiel, L Faivre, L Wilson, et al.
Pageof 23

Showing results (91-100 of 223) with videos related to

Sort By:
Pageof 23
L'Encephale|November 25, 2018
[Child psychiatry interventions in patients with 22q11 deletion syndrome: From treatment to prevention]A Novo, L Woestelandt, B Rousselot-Pailley, et al.
American Journal of Human Genetics|April 29, 1998
Mutations of the RET-GDNF signaling pathway in Ondine's curseJ Amiel, R Salomon, T Attié, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1996
[Isolated neonatal dysfunction of brainstem]V Abadie, G Chéron, S Lyonnet, et al.
Journal of Medical Genetics|July 31, 2001
B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?P Edery, F Le Deist, M L Briard, et al.
American Journal of Medical Genetics|January 30, 1995
Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?P Saugier-Veber, A Munnich, S Lyonnet, et al.
American Journal of Medical Genetics|October 15, 1994
Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindredE Dow, S Cross, D J Wolgemuth, et al.
Journal of Medical Genetics|March 10, 2001
MECP2 mutation in non-fatal, non-progressive encephalopathy in a maleB Imessaoudene, J P Bonnefont, G Royer, et al.
European Journal of Biochemistry|April 15, 1989
Apolipoprotein-E-gene expression in rat liver during development in relation to insulin and glucagonM Mangeney, P Cardot, S Lyonnet, et al.
American Journal of Medical Genetics|March 17, 1997
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeV Cormier-Daire, M Le Merrer, N Gigarel, et al.
Journal of Medical Genetics|February 12, 2002
Dysmorphism, variable overgrowth, normal bone age, and severe developmental delay: a "Sotos-like" syndrome?J Amiel, L Faivre, L Wilson, et al.
Pageof 23