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

rG. Potential pitfall in parentage testing.

J L Schornack, K M Beattie

    Transfusion
    |May 1, 1985
    PubMed
    Summary
    This summary is machine-generated.

    Accurate genetic testing for hemolytic disease of the newborn (HDN) is crucial. This study highlights how specific Rh gene testing prevented false paternity and maternity exclusions in a large Caucasian family.

    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

    Listen to employees!

    Fund raising management·1995
    Same author

    The Kmod blood group phenotype in a healthy individual.

    Transfusion·1989
    Same author

    Transient reduction in erythrocyte membrane sialoglycoprotein beta associated with the presence of elliptocytes.

    British journal of haematology·1988
    Same author

    Erb, an allele to Era, and evidence for a third allele, Er.

    Transfusion·1988
    Same author

    A Ge-like autoantibody in the serum of a patient receiving gold therapy for rheumatoid arthritis.

    Transfusion·1987
    Same author

    The immunohematology consultation report: what, when, how much?

    Immunohematology·1987
    Same journal

    Spray dried plasma manufactured from apheresis and whole blood derived plasma.

    Transfusion·2026
    Same journal

    Identification of a novel ABO*A1.01 allele with c.562C>T (p.Arg188Cys) mutation associated with A<sub>el</sub> phenotype in a Chinese individual.

    Transfusion·2026
    Same journal

    AABB survey on directed blood donation practices.

    Transfusion·2026
    Same journal

    Cost analysis considerations for red blood cell matching to mitigate alloimmunization in patients with sickle cell disease.

    Transfusion·2026
    Same journal

    A novel translation initiation codon single nucleotide variant of the SLC14A1 (c.2T>G) from a Chinese blood donor with Jk(a-b-) phenotype.

    Transfusion·2026
    Same journal

    Size (and frequency) matter: Evaluating the best management practices for blood products with spotty demand.

    Transfusion·2026
    See all related articles

    Area of Science:

    • Genetics
    • Immunology
    • Pediatrics

    Background:

    • Hemolytic disease of the newborn (HDN) is a serious condition.
    • Accurate genetic and serological testing is vital for diagnosis and family studies.
    • Rh blood group system plays a significant role in HDN.