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

A Moncla

Showing results (21-30 of 51) with videos related to

Pageof 6
Sort By:
European Journal of Pediatrics|February 9, 2000
Costello syndrome: report of six patients including one with an embryonal rhabdomyosarcomaS Sigaudy, G Vittu, A David, et al.
Journal of Medical Genetics|March 1, 1997
Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studiesC Mignon, F Parente, C Stavropoulou, et al.
Human Genetics|February 1, 1993
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeA Moncla, L Piras, O F Arbex, et al.
Pediatrie|January 1, 1992
[Molecular biology in genetic counseling of Duchenne and Becker myopathy]N Philip, M A Voelckel, L Girardot, et al.
Human Genetics|March 1, 1992
Physical mapping of an Xq-proximal interstitial duplication in a maleF Muscatelli, J M Verna, N Philip, et al.
European Journal of Pediatrics|January 1, 1993
Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literatureA Verloes, C Elmer, D Lacombe, et al.
American Journal of Human Genetics|July 1, 1994
Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicapS J Knight, M A Voelckel, M C Hirst, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1994
[Angelman syndrome]A Moncla, M O Livet, P Malzac, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
European Journal of Pediatrics|February 9, 2000
Costello syndrome: report of six patients including one with an embryonal rhabdomyosarcomaS Sigaudy, G Vittu, A David, et al.
Journal of Medical Genetics|March 1, 1997
Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studiesC Mignon, F Parente, C Stavropoulou, et al.
Human Genetics|February 1, 1993
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeA Moncla, L Piras, O F Arbex, et al.
Pediatrie|January 1, 1992
[Molecular biology in genetic counseling of Duchenne and Becker myopathy]N Philip, M A Voelckel, L Girardot, et al.
Human Genetics|March 1, 1992
Physical mapping of an Xq-proximal interstitial duplication in a maleF Muscatelli, J M Verna, N Philip, et al.
European Journal of Pediatrics|January 1, 1993
Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literatureA Verloes, C Elmer, D Lacombe, et al.
American Journal of Human Genetics|July 1, 1994
Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicapS J Knight, M A Voelckel, M C Hirst, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1994
[Angelman syndrome]A Moncla, M O Livet, P Malzac, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
Pageof 6