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

Neonatal Proteus syndrome?

Atia G Mohamedbhai, A M Hassan Miyan, Didier Lacombe

    American Journal of Medical Genetics
    |September 24, 2002
    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

    De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity.

    Nature communications·2026
    Same author

    Treatment-related benefit and satisfaction in patients with Fabry disease in France: insight into patients' expectations and preferences from the prospective, non-interventional SATIS-Fab study.

    Orphanet journal of rare diseases·2026
    Same author

    Cost-Effectiveness and Public Health Impact of Newborn Screening for Spinal Muscular Atrophy in France.

    Applied health economics and health policy·2026
    Same author

    Non-coding genome in nail-patella syndrome: Genetic diagnosis as a guide for personalized follow-up.

    European journal of human genetics : EJHG·2026
    Same author

    Phenotypic description of a large French series of individuals with Potocki-Lupski syndrome.

    Journal of medical genetics·2026
    Same author

    Prominent U-waves without QT prolongation in X-linked creatine transporter deficiency caused by SLC6A8 variants.

    Heart rhythm·2025