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

L M Curfs

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
Patient Education and Counseling|June 24, 2000
Psychosocial problems, coping strategies, and the need for information of parents of children with Prader-Willi syndrome and Angelman syndromeH W van den Borne, R H van Hooren, M van Gestel, et al.
The American Journal of Clinical Nutrition|March 4, 2000
Energy expenditure at rest and during sleep in children with Prader-Willi syndrome is explained by body compositionE A van Mil, K R Westerterp, W J Gerver, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 11, 2000
Activity related energy expenditure in children and adolescents with Prader-Willi syndromeE G van Mil, K R Westerterp, A D Kester, et al.
American Journal of Medical Genetics|April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?G S Fisch, L R Shapiro, R Simensen, et al.
American Journal of Medical Genetics|February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter studyG S Fisch, T Arinami, U Froster-Iskenius, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Mental status and fragile X expression in relation to FMR-1 gene mutationB B de Vries, A M Wiegers, E de Graaff, et al.
Neurogenetics|October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)C D Coldren, Z Lai, P Shragg, et al.
American Journal of Human Genetics|May 1, 1996
Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Patient Education and Counseling|June 24, 2000
Psychosocial problems, coping strategies, and the need for information of parents of children with Prader-Willi syndrome and Angelman syndromeH W van den Borne, R H van Hooren, M van Gestel, et al.
The American Journal of Clinical Nutrition|March 4, 2000
Energy expenditure at rest and during sleep in children with Prader-Willi syndrome is explained by body compositionE A van Mil, K R Westerterp, W J Gerver, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 11, 2000
Activity related energy expenditure in children and adolescents with Prader-Willi syndromeE G van Mil, K R Westerterp, A D Kester, et al.
American Journal of Medical Genetics|April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?G S Fisch, L R Shapiro, R Simensen, et al.
American Journal of Medical Genetics|February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter studyG S Fisch, T Arinami, U Froster-Iskenius, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Mental status and fragile X expression in relation to FMR-1 gene mutationB B de Vries, A M Wiegers, E de Graaff, et al.
Neurogenetics|October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)C D Coldren, Z Lai, P Shragg, et al.
American Journal of Human Genetics|May 1, 1996
Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.
Pageof 3