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Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Resolution of translation start site for the human Kell glycoprotein.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2882, doi. 10.1111/trf.12267
- By:
- Publication type:
- Article
Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Three novel alleles in the Kell blood group system resulting in the K<sub>null</sub> phenotype and the first in a Native American.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2867, doi. 10.1111/trf.12205
- By:
- Publication type:
- Article
P(1) /P(2) genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.
- Published in:
- 2013
- By:
- Publication type:
- journal article
A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Molecular background of novel silent RHCE alleles.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2990, doi. 10.1111/trf.12023
- By:
- Publication type:
- Article
Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2834, doi. 10.1111/trf.12411
- By:
- Publication type:
- Article
New RHCE variant alleles encoding the D- - phenotype.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 3018, doi. 10.1111/trf.12404
- By:
- Publication type:
- Article
Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2910, doi. 10.1111/trf.12168
- By:
- Publication type:
- Article
A convenient qualitative and quantitative method to investigate RHD- RHCE hybrid genes.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2974, doi. 10.1111/trf.12179
- By:
- Publication type:
- Article
The concept of 'confirmatory testing' of donors for ABO and RhD.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2837, doi. 10.1111/trf.12413
- By:
- Publication type:
- Article
Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 ( DARE), and DARA.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 3000, doi. 10.1111/trf.12363
- By:
- Publication type:
- Article
Proficiency testing for blood group genotyping.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2847, doi. 10.1111/trf.12408
- By:
- Publication type:
- Article
RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr<sup>S</sup>-, hr<sup>B</sup>-, RH:-61 phenotype in black persons: clinical significance.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2983, doi. 10.1111/trf.12271
- By:
- Publication type:
- Article
Identification of novel silent KEL alleles causing KEL:−5 ( Ko) phenotype or discordance between KEL:1,−2 phenotype/ KEL*01/02 genotype.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2859, doi. 10.1111/trf.12206
- By:
- Publication type:
- Article
Next-generation sequencing: proof of concept for antenatal prediction of the fetal Kell blood group phenotype from cell-free fetal DNA in maternal plasma.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2892, doi. 10.1111/trf.12172
- By:
- Publication type:
- Article
Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2899, doi. 10.1111/trf.12410
- By:
- Publication type:
- Article
External quality assessment in molecular immunohematology: the INSTAND proficiency test program.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2850, doi. 10.1111/trf.12414
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- Publication type:
- Article
Nomenclature for red blood cell blood group alleles.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2844, doi. 10.1111/trf.12407
- By:
- Publication type:
- Article
RHD variants in Polish blood donors routinely typed as D-.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2945, doi. 10.1111/trf.12230
- By:
- Publication type:
- Article
P<sup>1</sup>/ P<sup>2</sup> genotyping of known and novel null alleles in the P1 PK and GLOB histo-blood group systems.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2928, doi. 10.1111/trf.12355
- By:
- Publication type:
- Article
Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K<sub>0</sub> ( Kell<sub>null</sub>) phenotypes.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2887, doi. 10.1111/trf.12377
- By:
- Publication type:
- Article
Where are we in efforts to unravel the complexity of Rh to guide transfusion decisions?
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2840, doi. 10.1111/trf.12406
- By:
- Publication type:
- Article
Molecular basis of two novel and related high-prevalence antigens in the Kell blood group system, KUCI and KANT, and their serologic and spatial association with K11 and KETI.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2872, doi. 10.1111/trf.12200
- By:
- Publication type:
- Article
Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a B<sub>m</sub> subgroup individual.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2917, doi. 10.1111/trf.12181
- By:
- Publication type:
- Article
A novel JK*02 allele in a French Canadian family.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 3024, doi. 10.1111/trf.12266
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- Publication type:
- Article
D category IV: a group of clinically relevant and phylogenetically diverse partial D.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2960, doi. 10.1111/trf.12145
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- Publication type:
- Article
A historical perspective on the discovery of the Kell blood group carriers.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2831, doi. 10.1111/trf.12405
- By:
- Publication type:
- Article
A comprehensive survey of both RHD and RHCE allele frequencies in sub- Saharan Africa.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 3009, doi. 10.1111/trf.12409
- By:
- Publication type:
- Article
Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2940, doi. 10.1111/trf.12100
- By:
- Publication type:
- Article
Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2954, doi. 10.1111/trf.12180
- By:
- Publication type:
- Article