Works matching AU Veldhuisen, Barbera
Results: 21
Prevalence of RhD status and clinical application of non-invasive prenatal determination of fetal RHD in maternal plasma: a 5 year experience in Cyprus.
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- BMC Research Notes, 2016, v. 9, p. 1, doi. 10.1186/s13104-016-2002-x
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- Publication type:
- Article
Location of mutations within the PKD2 gene influences clinical outcome.
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- Kidney International, 2000, v. 57, n. 4, p. 1444, doi. 10.1046/j.1523-1755.2000.00989.x
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- Publication type:
- Article
Performance evaluation study of ID RHD XT, a new genotyping assay for the detection of high‐prevalence RhD negative and weak D types.
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- Vox Sanguinis, 2018, v. 113, n. 7, p. 694, doi. 10.1111/vox.12701
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- Article
Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D-negative pregnant women.
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- British Journal of Haematology, 2016, v. 173, n. 3, p. 469, doi. 10.1111/bjh.13960
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- Publication type:
- Article
PIGG defines the Emm blood group system.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98090-w
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- Publication type:
- Article
Novel variants in Krueppel like factor 1 that cause persistence of fetal hemoglobin in In(Lu) individuals.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-97149-y
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- Publication type:
- Article
Rh‐null phenotype and stomatocytosis.
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- British Journal of Haematology, 2021, v. 194, n. 5, p. 803, doi. 10.1111/bjh.17486
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- Article
Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2).
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- European Journal of Human Genetics, 1999, v. 7, n. 8, p. 860, doi. 10.1038/sj.ejhg.5200383
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- Publication type:
- Article
Performance evaluation study of ID CORE XT, a high throughput blood group genotyping platform.
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- Blood Transfusion (17232007), 2018, v. 16, n. 2, p. 193, doi. 10.2450/2016.0146-16
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- Publication type:
- Article
Identification of a novel single-nucleotide mutation in SMIM1 gene that results in low Vel antigen expression.
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- 2019
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- Publication type:
- journal article
Frequency and characterization of RHD variants in serologically D- Surinamese pregnant women and D- newborns.
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- 2019
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- Publication type:
- journal article
Development of a recombinant anti-Vel immunoglobulin M to identify Vel-negative donors.
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- 2019
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- Publication type:
- journal article
Validation of the multiplex ligation-dependent probe amplification assay and its application on the distribution study of the major alleles of 17 blood group systems in Chinese donors from Guangzhou.
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- 2017
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- Publication type:
- journal article
Identification of a novel frequent RHCE*ce308T variant allele in Chinese D- individuals, resulting in a C+c- phenotype.
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- 2016
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- Publication type:
- journal article
Fetal RHD genotyping after bone marrow transplantation.
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- 2016
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- Publication type:
- Case Study
Will Genotyping Replace Serology in Future Routine Blood Grouping? – Opinion 5.
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- Transfusion Medicine & Hemotherapy, 2009, v. 36, n. 3, p. 234, doi. 10.1159/000214840
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- Publication type:
- Article
Novel alleles at the Kell blood group locus that lead to Kell variant phenotype in the Dutch population.
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- Transfusion, 2015, v. 55, n. 2, p. 413, doi. 10.1111/trf.12838
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- Publication type:
- Article
Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience.
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- Transfusion, 2013, v. 53, n. 11pt2, p. 2834, doi. 10.1111/trf.12411
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- Publication type:
- Article
Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy.
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- Transfusion, 2013, v. 53, n. 11pt2, p. 2899, doi. 10.1111/trf.12410
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- Publication type:
- Article
RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.
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- Transfusion, 2013, v. 53, n. 7, p. 1559, doi. 10.1111/j.1537-2995.2012.03919.x
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- Publication type:
- Article
Molecular analysis of the York antigen of the Knops blood group system.
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- Transfusion, 2011, v. 51, n. 7, p. 1389, doi. 10.1111/j.1537-2995.2010.02999.x
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- Publication type:
- Article