Abstract
L'auteur discute et présente, à la lumière des douze observations actuellement connues, la revue générale des problèmes fondamentaux soulevés par le phénotype Rh nul, en particulier son déterminisme génétique, ses inter-relations phénotypiques et le défaut associé de l'intégrité de la membrane érythrocytaire. Some fundamental problems of the Rh null phenotype, especially its genetic pathways, its phenotypic interactions and the associated red cell membrane defect, are discussed in the light of data obtained from the twelve so far known families.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callSimilar Papers
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
