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. 2022 Aug;62(8):E37-E39.
doi: 10.1111/trf.17009. Epub 2022 Jul 14.

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman

Cecilia Pardi  1 , Åsa Hellberg  2 , Marieta Kapadzha  1 , Martin L Olsson  2   3 , Pauline Isakson  1
Affiliations

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman

Cecilia Pardi et al. Transfusion. 2022 Aug.
No abstract available

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References

REFERENCES

    1. Daniels G. Variants of RhD - current testing and clinical consequences. Br J Haematol. 2013;161:461-70.
    1. Raud L, Férec C, Fichou Y. From genetic variability to phenotypic expression of blood group systems. Transfus Clin Biol. 2017;24:472-5.
    1. Wikman AT, Tiblad E, Karlsson A, Olsson ML, Westgren M, Reilly M. Noninvasive single-exon fetal RHD determination in a routine screening program in early pregnancy. Obstet Gynecol. 2012;120:227-34.
    1. Singleton BK, Green CA, Avent ND, Martin PG, Smart E, Daka A, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype. Blood. 2000;95:12-8.
    1. Gassner C, Schmarda A, Kilga-Nogler S, Jenny-Feldkircher B, Rainer E, Muller TH, et al. RHD/CE typing by polymerase chain reaction using sequence-specific primers. Transfusion. 1997;37:1020-6.

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