Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.

Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.

Item
http://www.wikidata.org/entity/Q34132155
RHD variants in Polish blood donors routinely typed as D-Prospective Evaluation of a Transfusion Policy of RhD-Positive Red Blood Cells into DEL Patients in ChinaPrevalence of RhD status and clinical application of non-invasive prenatal determination of fetal RHD in maternal plasma: a 5 year experience in Cyprus.Anti-D alloimmunisation in pregnant women with DEL phenotype in China.Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.A new strategy to identify rare blood donors: single polymerase chain reaction multiplex SNaPshot reaction for detection of 16 blood group alleles.RHD variants in Flanders, Belgium.Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare alleles.Weak D caused by a founder deletion in the RHD gene.Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.Two large deletions extending beyond either end of the RHD gene and their red cell phenotypes.The synonymous nucleotide substitution RHD 1056C>G alters mRNA splicing associated with serologically weak D phenotype.First description of a D-CE-D hybrid gene on a weak D Type 2 molecular background.Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles.New silent and weak D alleles: molecular characterization and associated antigen density.Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.
P2860

Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.

Item
http://www.wikidata.org/entity/Q34132155
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@ast
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@en
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@nl
type
label
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@ast
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@en
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@nl
prefLabel
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@ast
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@en
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P5875
P698
P356
P1433
P1476
Weak D and DEL alleles detecte ...... ion of four novel RHD alleles.
@en
P2093
P2860
P304
P31
P356
10.1111/J.1537-2995.2010.02830.X
P433
P478
P577
P5875
P698