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

Related Experiment Videos

Genomic imprinting in humans

D J Driscoll1

  • 1Department of Pediatrics, University of Florida College of Medicine, Gainesville 32610.

Molecular Genetic Medicine
|January 1, 1994
PubMed
Summary

No abstract available in PubMed .

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The presentation, course and outcome of COVID-19 infection in people with Prader-Willi syndrome: unexpected findings from an international survey.

Orphanet journal of rare diseases·2022
Same author

Skin-Related complications of Klippel-Trenaunay Syndrome: a retrospective review of 410 patients.

Journal of the European Academy of Dermatology and Venereology : JEADV·2020
Same author

EVALUATION OF PLASMA SUBSTANCE P AND BETA-ENDORPHIN LEVELS IN CHILDREN WITH PRADER-WILLI SYNDROME.

The Journal of rare disorders·2016
Same author

A reduced-energy intake, well-balanced diet improves weight control in children with Prader-Willi syndrome.

Journal of human nutrition and dietetics : the official journal of the British Dietetic Association·2012
Same author

Epigenetic regulation of pericentromeric heterochromatin during mammalian meiosis.

Cytogenetic and genome research·2010
Same author

Identification of association of common AGGF1 variants with susceptibility for Klippel-Trenaunay syndrome using the structure association program.

Annals of human genetics·2008
Same journal

Superoxide dismutase, oxygen radical metabolism, and amyotrophic lateral sclerosis.

Molecular genetic medicine·1994
Same journal

Impact of gene targeting on medicine.

Molecular genetic medicine·1994
Same journal

Protein import deficiencies in human peroxisomal disorders.

Molecular genetic medicine·1994
Same journal

Molecular genetics of blindness.

Molecular genetic medicine·1994
Same journal

Molecular biology of Alzheimer's disease.

Molecular genetic medicine·1993
Same journal

Genetics of astrocytic tumor progression.

Molecular genetic medicine·1993
See all related articles