Literature DB >> 17655603

IVS5-38del4 deletion in the RHD gene does not cause a DEL phenotype: relevance for RHD alleles including DFR-3.

Inge von Zabern, Willy A Flegel.   

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Year:  2007        PMID： 17655603     DOI： 10.1111/j.1537-2995.2007.01353.x

Source DB:  PubMed          Journal:  Transfusion        ISSN： 0041-1132            Impact factor:   3.157


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  6 in total

1.  RHD PCR of D-Negative Blood Donors.

Authors:  Franz F Wagner
Journal:  Transfus Med Hemother       Date:  2013-05-08       Impact factor: 3.747

2.  Prospective Evaluation of a Transfusion Policy of RhD-Positive Red Blood Cells into DEL Patients in China.

Authors:  Wei Xu; Mei Zhu; Bao-Long Wang; Hong Su; Min Wang
Journal:  Transfus Med Hemother       Date:  2014-12-22       Impact factor: 3.747

3.  Application of a Multivariant, Caucasian-Specific, Genotyped Donor Panel for Performance Validation of MDmulticard®, ID-System®, and Scangel® RhD/ABO Serotyping.

Authors:  Christoph Gassner; Esther Rainer; Elfriede Pircher; Lydia Markut; Günther F Körmöczi; Christof Jungbauer; Dietmar Wessin; Roswitha Klinghofer; Harald Schennach; Peter Schwind; Diether Schönitzer
Journal:  Transfus Med Hemother       Date:  2009-05-18       Impact factor: 3.747

4.  DEL phenotype.

Authors:  Dong H Kwon; S G Sandler; Willy A Flegel
Journal:  Immunohematology       Date:  2017-09

5.  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

6.  Two distinct RHCE alleles in cis to weak D type 31 alleles in individuals from different ethnicities.

Authors:  Kshitij Srivastava; Günther F Körmöczi; Sanmukh R Joshi; Willy A Flegel
Journal:  Transfusion       Date:  2018-09-24       Impact factor: 3.157
  6 in total

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