Literature DB >> 33270227

A null allele caused by a four-base-pair duplication within the RHCE gene encoding a D- - phenotype.

Qing Chen1,2, Jianyu Xiao1, Min Zhang3, Chengyin Huang1, Min Li2,4, Willy A Flegel5,6, Xiaoyu Zhou3.   

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Year:  2020        PMID： 33270227      PMCID： PMC9066653          DOI： 10.1111/trf.16211

Source DB:  PubMed          Journal:  Transfusion        ISSN： 0041-1132            Impact factor:   3.337


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  4 in total

1.  Successful management of fetal hemolytic disease due to strong anti-Rh17 with plasma exchange and intrauterine transfusion in a woman with the D-- phenotype.

Authors:  Kazuya Mimura; Masayuki Endo; Atsushi Takahashi; Yohei Doi; Mikiko Sakuragi; Tomoko Kiyokawa; Hidetoshi Taniguchi; Yasuji Kitabatake; Mika Handa; Takuji Tomimatsu; Yoshiaki Tomiyama; Yoshitaka Isaka; Tadashi Kimura
Journal:  Int J Hematol       Date:  2019-09-19       Impact factor: 2.490

2.  Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.

Authors:  Monique Silvy; Sophie Beley; Thierry Peyrard; Mouna Ouchari; Saadia Abdelkefi; Saloua Jemni Yacoub; Jacques Chiaroni; Pascal Bailly
Journal:  Transfusion       Date:  2014-11-21       Impact factor: 3.157

3.  RhCE protein variants in Southwestern Germany detected by serologic routine testing.

Authors:  Peter Bugert; Erwin A Scharberg; Christof Geisen; Inge von Zabern; Willy A Flegel
Journal:  Transfusion       Date:  2009-05-18       Impact factor: 3.157

Review 4.  The Outcome of Hemolytic Disease of the Fetus and Newborn Caused by Anti-Rh17 Antibody: Analysis of Three Cases and Review of the Literature.

Authors:  Slavica Dajak; Nina Ipavec; Mia Cuk; Branka Golubic Cepulic; Jela Mratinovic-Mikulandra; Josipa Milardovic; Vedran Stefanovic
Journal:  Transfus Med Hemother       Date:  2019-10-03       Impact factor: 3.747
  4 in total

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