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

X-linked dominant ichthyosis

R Happle

    Clinical Genetics
    |March 1, 1979
    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

    Frontal fibrosing alopecia sparing a dermal melanocytic nevus: a report of two cases of Renbök phenomenon.

    Journal of the European Academy of Dermatology and Venereology : JEADV·2022
    Same author

    White lentiginosis of Grosshans: which mode of inheritance?

    Journal of the European Academy of Dermatology and Venereology : JEADV·2021
    Same author

    Phylloid hypermelanosis: further report of an unusual syndrome.

    Journal of the European Academy of Dermatology and Venereology : JEADV·2021
    Same author

    Two examples of Renbök phenomenon in dermatophytosis sparing congenital nevi.

    Journal of the European Academy of Dermatology and Venereology : JEADV·2021
    Same author

    A proposed new category of cutaneous segmental mosaicism: Isolated segmental biallelic monoclonal mosaicism.

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

    Flag-like hypermelanosis with superimposed lichen sclerosus et atrophicus: an unusual Koebner phenomenon?

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

    Diagnostic Yield and Clinical Impact of Comprehensive WES/WGS Testing Beyond Common Genetic Causes in Hereditary Optic Atrophy.

    Clinical genetics·2026
    Same journal

    Further Support of Autosomal Recessive CSF3-Related Severe Congenital Neutropenia.

    Clinical genetics·2026
    Same journal

    Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in Nephrology: A Response Letter.

    Clinical genetics·2026
    Same journal

    Research Progress on the Pathogenesis and Diagnostic and Therapeutic Potential of Ciliopathies Regulated by IFT172.

    Clinical genetics·2026
    Same journal

    Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants.

    Clinical genetics·2026
    Same journal

    Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature.

    Clinical genetics·2026
    See all related articles