Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Lyonnet

Showing results (1-10 of 223) with videos related to

Pageof 23
Sort By:
Pediatrie|January 1, 1987
[A strategy for studying a mutation]S Lyonnet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 27, 2003
[Impact of genetic information about diseases "not like the others"]S Lyonnet, A Munnich
Journal of Medical Genetics|November 6, 2001
Hirschsprung disease, associated syndromes, and genetics: a reviewJ Amiel, S Lyonnet
Archives Francaises De Pediatrie|May 1, 1991
[Correlations between genotype and phenotype in children with phenylketonuria?]P Labrune, S Lyonnet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Grandparents and genetics]M C Nolen, S Lyonnet
European Journal of Human Genetics : EJHG|January 1, 1995
Israel-France binational symposium on 'hereditary diseases, molecular diagnosis and gene therapy'S Lyonnet, A Brice, J Zlotogora
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 6, 2010
[Malformation syndromes associated with childhood cancer: an update]L de Pontual, S Lyonnet, J Amiel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 17, 2007
[Genetic and molecular bases of neurocristopathies]H-C Etchevers, J Amiel, S Lyonnet
Trends in Genetics : TIG|September 28, 1999
Genetics of limb anomalies in humansS Manouvrier-Hanu, M Holder-Espinasse, S Lyonnet
Archives Francaises De Pediatrie|January 1, 1987
[Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency]F Rey, A Munnich, S Lyonnet, et al.
Pageof 23

Showing results (1-10 of 223) with videos related to

Sort By:
Pageof 23
Pediatrie|January 1, 1987
[A strategy for studying a mutation]S Lyonnet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 27, 2003
[Impact of genetic information about diseases "not like the others"]S Lyonnet, A Munnich
Journal of Medical Genetics|November 6, 2001
Hirschsprung disease, associated syndromes, and genetics: a reviewJ Amiel, S Lyonnet
Archives Francaises De Pediatrie|May 1, 1991
[Correlations between genotype and phenotype in children with phenylketonuria?]P Labrune, S Lyonnet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Grandparents and genetics]M C Nolen, S Lyonnet
European Journal of Human Genetics : EJHG|January 1, 1995
Israel-France binational symposium on 'hereditary diseases, molecular diagnosis and gene therapy'S Lyonnet, A Brice, J Zlotogora
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 6, 2010
[Malformation syndromes associated with childhood cancer: an update]L de Pontual, S Lyonnet, J Amiel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 17, 2007
[Genetic and molecular bases of neurocristopathies]H-C Etchevers, J Amiel, S Lyonnet
Trends in Genetics : TIG|September 28, 1999
Genetics of limb anomalies in humansS Manouvrier-Hanu, M Holder-Espinasse, S Lyonnet
Archives Francaises De Pediatrie|January 1, 1987
[Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency]F Rey, A Munnich, S Lyonnet, et al.
Pageof 23