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

[True and false regarding the genetic risks in contraception]

C Moraine

    Contraception, Fertilite, Sexualite
    |November 1, 1981
    PubMed
    Summary

    No abstract available in PubMed .

    Keywords:
    Abortion, SpontaneousBiologyBirth WeightBody WeightChromosome AbnormalitiesCongenital AbnormalitiesContraceptionContraception FailureContraceptive Methods--side effectsContraceptive UsageDemographic FactorsDiseasesFamily PlanningFetal DeathGeneticsLiterature ReviewMaternal AgeMortalityNeonatal Diseases And AbnormalitiesOral Contraceptives--side effectsPhysiologyPopulationPopulation CharacteristicsPopulation DynamicsPregnancyPregnancy ComplicationsPregnancy OutcomesReproductionSex DistributionSex FactorsSex RatioSocioeconomic Factors

    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 and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.

    Molecular psychiatry·2016
    Same author

    Twenty-five novel mutations including duplications in the ATP7A gene.

    Clinical genetics·2011
    Same author

    Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism.

    Molecular psychiatry·2009
    Same author

    Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis.

    Neurogenetics·2005
    Same author

    Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia.

    Neurology·2005
    Same author

    Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate.

    Journal of medical genetics·2005