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

Partial monosomy 10p syndrome.

R Koenig, E Kessel, W Schoenberger

    Annales De Genetique
    |January 1, 1985
    PubMed
    Summary
    This summary is machine-generated.

    A newborn infant with monosomy 10p13 was identified. Comparing this case with others suggests a recognizable pattern of clinical features, even without a single defining symptom.

    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

    Neural network surrogates of Bayesian diagnostic models for fast inference of plasma parameters.

    The Review of scientific instruments·2021
    Same author

    Investigation of boron carbide and iridium thin films, an enabling technology for future x-ray telescopes.

    Applied optics·2020
    Same author

    First Report of Soilborne Rye Mosaic Virus in Rye in Denmark.

    Plant disease·2019
    Same author

    Petunia vein banding virus: Characterization of a New Tymovirus from Petunia × hybrida.

    Plant disease·2019
    Same author

    Quinacrine sterilization: a retrospective.

    International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics·2018
    Same author

    Detection and Characterization of a Distinct Type of Beet Necrotic Yellow Vein Virus RNA 5 in a Sugarbeet Growing Area in Europe.

    Archives of virology·2017
    Same journal

    Effect of 5637 conditioned medium (CM) on the mitotic index in the cytogenetic evaluation of myeloproliferative disorders.

    Annales de genetique·2004
    Same journal

    Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

    Annales de genetique·2004
    Same journal

    Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

    Annales de genetique·2004
    Same journal

    Large duplication 4q25-q34 with mild clinical effect.

    Annales de genetique·2004
    Same journal

    A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

    Annales de genetique·2004
    Same journal

    Partial trisomy 8q and partial monosomy 18p: a case report.

    Annales de genetique·2004
    See all related articles

    Area of Science:

    • Genetics
    • Pediatrics
    • Clinical Medicine

    Background:

    • Monosomy 10p13 is a rare chromosomal abnormality.
    • Understanding the clinical spectrum of partial deletions of chromosome 10p is crucial for diagnosis and management.

    Observation:

    • A case report of a newborn infant diagnosed with monosomy 10p13 is presented.
    • Detailed clinical signs and symptoms of the infant were recorded.

    Findings:

    • Comparison with previously reported cases of monosomy 10p indicates a recognizable, albeit non-pathognomonic, syndrome.
    • Specific phenotypic features associated with monosomy 10p13 deletions are being delineated.

    Implications:

    • This case contributes to the growing knowledge base of monosomy 10p syndromes.
  • Further research can refine diagnostic criteria and inform genetic counseling for families affected by 10p deletions.