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- Arnoni CP et al. Identification of four novel RHD alleles with altered expression of D in Brazilians. Transfusion, 2016. [Citation] [RHeference]
- Zhao H et al. A serologic weakly reactive RhD is caused by a c.496C>G (p.His166Asp) in RHD gene. Transfusion, 2016. [Citation] [RHeference]
- C Nixon et al. A Patient with Weak D Type 3 and Anti-D Alloimmunization Transfusion, 2016. — Abstract — [RHeference]
- Srivastava K et al. The DAU cluster: a comparative analysis of 18 RHD alleles, some forming partial D antigens. Transfusion, 2016. [Citation] [RHeference]
- Yazer MH et al. Low incidence of D alloimmunization among patients with a serologic weak D phenotype after D+ transfusion. Transfusion, 2016. [Citation] [RHeference]
- Trucco Boggione C et al. Weak D antigen expression caused by a novel RHD allele in Argentineans. Transfusion, 2016. [Citation] [RHeference]
- Filosa L et al. New silent and weak D alleles: molecular characterization and associated antigen density. Transfusion, 2016. [Citation] [RHeference]
- Polin H et al. RHD Tyr311Stop encoded by a novel nonsense mutation. Transfusion, 2016. [Citation] [RHeference]
- Fennell K et al. Effect on gene expression of three allelic variants in GATA motifs of ABO, RHD, and RHCE regulatory elements. Transfusion, 2017. [Citation] [RHeference]
- Bruno Costes et al. c.1154-31C>T Is in Linkage Disequilibrium with the Missense Mutation C.1154G>C on RHD Weak Type 2 Transfusion, 2017. — Abstract — [RHeference]
- Granier T et al. First description of a D-CE-D hybrid gene on a weak D Type 2 molecular background. Transfusion, 2017. [Citation] [RHeference]
- J P Hudgins et al. Serologic and Molecular Classification of a Novel RHD Allele Transfusion, 2017. — Abstract — [RHeference]
- S Vege et al. Expansion of the RHD DAU Cluster: Identification of Two Additional Novel Alleles Transfusion, 2017. — Abstract — [RHeference]
- S Vege et al. Serologic Characterization of D Antigen Expression Encoded By Two Reported RHD Alleles: Implications for Transfusion and Pregnancy Transfusion, 2017. — Abstract — [RHeference]
- S Vege et al. RHD Genotyping of Discrepant or Weak D Samples: Over a Year’s Experience. Transfusion, 2017. — Abstract — [RHeference]
- J Aeschlimann et al. Gene Conversion within the r’S Haplotype Complicates RHD Genotype Interpretations Transfusion, 2017. — Abstract — [RHeference]
- Floch A et al. Molecular characterization of 13 new RHD alleles. Transfusion, 2017. [Citation] [RHeference]
- Jérôme Babinet et al. Inscription des individus RH : −1, −4 ou RH : −1, −5 dans le registre national de référence des sujets présentant un phénotype/génotype érythrocytaire rare : intérêt de la réalisation d’une PCR multiplexe systématique pour le dépistage des variants RH1 affaiblis non détectés par sérologie de routine Transfusion Clinique et Biologique, 2017. — Abstract — [RHeference]
- Quantock KM et al. Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn. Transfusion, 2017. [Citation] [RHeference]
- Ouchari M et al. Serologic and molecular characterization of weak D type 29. Transfusion, 2017. [Citation] [RHeference]
- Anani WQ et al. Molecular characterization of three novel weak D type alleles with additional haplotype data on weak D Types 1.2 and 18. Transfusion, 2017. [Citation] [RHeference]
- Lopez GH et al. Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor. Transfusion, 2017. [Citation] [RHeference]
- Feng J et al. A new RHD variant allele is caused by a RHD 662C>G mutation. Transfusion, 2017. [Citation] [RHeference]
- Matteocci A et al. Two novel RHD alleles encoding truncated, nonfunctional D polypeptides. Transfusion, 2018. [Citation] [RHeference]
- Turley E et al. Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31). Transfusion, 2018. [Citation] [RHeference]
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- M. Ines Moser et al. A new RhD variant: DLO-Like? Transfusion Medicine, 2018. — Abstract — [RHeference]
- Schoeman EM et al. Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting. Transfusion, 2018. [Citation] [RHeference]
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- J Aeschlimann et al. Serological and Molecular Characterization of Three New RHD Alleles Transfusion, 2018. — Abstract — [RHeference]
- V L. Thonier et al. Complex Antibody Mixture in a Pregnant Woman Harboring the RHD*DIIIb Variant Allele Transfusion, 2018. — Abstract — [RHeference]
- C Araujo et al. Serological and Molecular Characterization of Weak D Type 18 in Four Brazilian Families Transfusion, 2018. — Abstract — [RHeference]
- J S. Woo et al. Robust Allo-Anti-D with Subsequent Anti-K Production after Transfusion of D-Positive RBCs to a Patient with Weak D Type 1 Transfusion, 2018. — Abstract — [RHeference]
- Jérôme Babinet et al. Erratum à l’article : « Résumés des Posters » [Transfus. Clin. Biol. 24 (2017) 3S] Transfusion Clinique et Biologique, 2018. — Abstract — [RHeference]
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- Srivastava K et al. Two distinct RHCE alleles in cis to weak D type 31 alleles in individuals from different ethnicities. Transfusion, 2018. [Citation] [RHeference]
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- de Brevern AG et al. Alloimmunization risk associated with amino acid 223 substitution in the RhD protein: analysis in the light of molecular modeling. Transfusion, 2018. [Citation] [RHeference]
- Polin H et al. Identification of four novel RHD alleles by weakened antigen D expression. Transfusion, 2018. [Citation] [RHeference]
- Zhang J et al. Identification of a novel missense mutation (p.Ser230Asn) in RHD allele in a Chinese individual with partial D phenotype. Transfusion, 2018. [Citation] [RHeference]
- Dezan MR et al. Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ. Transfusion, 2018. [Citation] [RHeference]
- Perez-Alvarez I et al. RHD genotyping of serologic RhD-negative blood donors in a hospital-based blood donor center. Transfusion, 2019. [Citation] [RHeference]
- Zhu Y et al. A new RHD variant allele in Exon 2 identified in a Chinese individual. Transfusion, 2019. [Citation] [RHeference]
- Qian C et al. A new RhD variant allele is caused by a RhD 26 T > G mutation in a Chinese Han woman with a weak D phenotype. Transfusion, 2019. [Citation] [RHeference]
- Sandler SG et al. Does transfusion of Asian-type DEL red blood cells to D- recipients cause D alloimmunization? Transfusion, 2019. [Citation] [RHeference]
- Izaskun Apraiz et al. Performance Evaluation Study of ID RHD XT as a Molecular Tool for RHD Gene Screening in Pooled Blood Samples of Serologically D− C/E+ Donors Transfusion, 2019. — Abstract — [RHeference]
- Trina Horn et al. Four Novel RHD Alleles Identified Through Investigation of Discrepant or Weak D Status Transfusion, 2019. — Abstract — [RHeference]
- Trina Horn et al. Two New RHD*Dau family Alleles Found in Three African American Patients Transfusion, 2019. — Abstract — [RHeference]
- Richard Garrett et al. Novel RHD-CE-D Hybrid Allele Associated With D- C+ Phenotype Transfusion, 2019. — Abstract — [RHeference]
- Matzhold EM et al. RHD del28Phe (DMW) encoded by a novel in-frame deletion resulting in reduced D antigen expression. Transfusion, 2019. [Citation] [RHeference]
- Sunitha Vege et al. Novel RHD Alleles Identified When Resolving Serologic Weak D Phenotypes Transfusion, 2019. — Abstract — [RHeference]
- Takeuchi-Baba C et al. Production of RBC autoantibody mimicking anti-D specificity following transfusion in a patient with weak D Type 15. Transfusion, 2019. [Citation] [RHeference]
- Trucco Boggione C et al. Characterization of RHD locus polymorphism in D negative and D variant donors from Northwestern Argentina. Transfusion, 2019. [Citation] [RHeference]
- Schoeman EM et al. Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data. Transfusion, 2019. [Citation] [RHeference]
- de Paula Vendrame TA et al. Novel RHD alleles in African Brazilians. Transfusion, 2019. [Citation] [RHeference]
- Stettler J et al. Reduced RhD antigen expression caused by two novel RHD variant alleles. Transfusion, 2020. [Citation] [RHeference]
- Mufarrege N et al. The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype. Transfusion, 2020. [Citation] [RHeference]
- Mathur G et al. A novel RHD*DAU allele with c.1136C>T (p.Thr379Met) and c.17C>T (p. Pro6Leu). Transfusion, 2020. [Citation] [RHeference]
- Srivastava K et al. NG_007494.1(RHD):c.[4A>T;5G>C;6_7insG] with an RhD-negative phenotype. Transfusion, 2020. [Citation] [RHeference]
- Jessica Keller et al. A Novel RHD Variant Identified in Two Pregnant Women with D Typing Discrepancies Transfusion, 2020. — Abstract — [RHeference]
- Sunitha Vege et al. Novel RHD Alleles and Predicting Risk for Anti-D Transfusion, 2020. — Abstract — [RHeference]
- Sunitha Vege et al. Novel RHCE*ceS with c.462G>T (p. Arg154Ser) Encodes Expression of a D Reactive Epitope Transfusion, 2020. — Abstract — [RHeference]
- Stef M et al. RH genotyping by nonspecific quantitative next-generation sequencing. Transfusion, 2020. [Citation] [RHeference]
- Chun S et al. A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants. Transfusion, 2020. [Citation] [RHeference]
- Deng D et al. Identification of a novel c.94dupA mutation in RHD allele. Transfusion, 2020. [Citation] [RHeference]
- Vege S et al. Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles. Transfusion, 2021. [Citation] [RHeference]
- Matteocci A et al. Two new RHD alleles with deletions spanning multiple exons. Transfusion, 2021. [Citation] [RHeference]
- Lyu H et al. A novel RHD allele caused by c.739 G> C mutation was identified in a Chinese individual. Transfusion, 2021. [Citation] [RHeference]