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

Trisomy 22

H Zellweger, V Ionasescu, J Simpson

    Journal De Genetique Humaine
    |October 1, 1975
    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

    About chronic abacterial meningitis.

    Annales paediatrici. International review of pediatrics·2010
    Same author

    About muscle hypotension.

    Annales paediatrici. International review of pediatrics·2010
    Same author

    Considerations on the 1944 poliomyelitis epidemic.

    Schweizerische medizinische Wochenschrift·2010
    Same author

    Sporadic case of constitutional, macrocytic anemia (Fanconi) in a 12 year old boy from a healthy family.

    Annales paediatrici. International review of pediatrics·2010
    Same author

    About two cases of congenital relaxation diaphragm with special consideration of the abdominal site.

    Helvetica paediatrica acta·2010
    Same author

    Twice poliomyelitis.

    Praxis·2010
    Same journal

    [Ultrasonic prenatal diagnosis of the Jarcho-Levin syndrome].

    Journal de genetique humaine·1989
    Same journal

    [Genetic mapping of chromosome X: known localizations].

    Journal de genetique humaine·1989
    Same journal

    [Animal models of gene therapy].

    Journal de genetique humaine·1989
    Same journal

    [The bases of genetic therapy].

    Journal de genetique humaine·1989
    Same journal

    Clinical and biological studies in 14 cases of Prader-Labhart Willi syndrome.

    Journal de genetique humaine·1989
    Same journal

    Paroxysmal intracranial hypertension and oculoauriculovertebral dysplasia.

    Journal de genetique humaine·1989
    See all related articles