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

R H Ardinger

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Pediatric Annals|February 1, 1997
Genetic counseling in congenital heart diseaseR H Ardinger
American Journal of Medical Genetics|July 1, 1994
Cerebrovascular stenoses with cerebral infarction in a child with Williams syndromeR H Ardinger, K K Goertz, L F Mattioli
American Journal of Medical Genetics|January 31, 1997
Cardiovascular malformations in Smith-Lemli-Opitz syndromeA E Lin, H H Ardinger, R H Ardinger, et al.
Telemedicine Journal : the Official Journal of the American Telemedicine Association|July 1, 1995
Evaluation of remote stethoscopy for pediatric telecardiologyJ M Belmont, L F Mattioli, K K Goertz, et al.
Genomics|January 1, 1989
Twenty-eight loci form a continuous linkage map of markers for human chromosome 1P O'Connell, G M Lathrop, Y Nakamura, et al.
Human Genetics|February 1, 1994
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21A J Cousineau, R M Lauer, M E Pierpont, et al.
Pediatric Cardiology|May 9, 2001
Iodixanol pharmacokinetics in childrenW H Johnson, T R Lloyd, B E Victorica, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Pediatric Annals|February 1, 1997
Genetic counseling in congenital heart diseaseR H Ardinger
American Journal of Medical Genetics|July 1, 1994
Cerebrovascular stenoses with cerebral infarction in a child with Williams syndromeR H Ardinger, K K Goertz, L F Mattioli
American Journal of Medical Genetics|January 31, 1997
Cardiovascular malformations in Smith-Lemli-Opitz syndromeA E Lin, H H Ardinger, R H Ardinger, et al.
Telemedicine Journal : the Official Journal of the American Telemedicine Association|July 1, 1995
Evaluation of remote stethoscopy for pediatric telecardiologyJ M Belmont, L F Mattioli, K K Goertz, et al.
Genomics|January 1, 1989
Twenty-eight loci form a continuous linkage map of markers for human chromosome 1P O'Connell, G M Lathrop, Y Nakamura, et al.
Human Genetics|February 1, 1994
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21A J Cousineau, R M Lauer, M E Pierpont, et al.
Pediatric Cardiology|May 9, 2001
Iodixanol pharmacokinetics in childrenW H Johnson, T R Lloyd, B E Victorica, et al.
Pageof 1