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[Serological and molecular study of RHD weak D expression mutant--a case report].

Zhonghua yi xue za zhi - 22 Jun 2005

Wu Jun-jie, Xu Xian-guo, Hong Xiao-zhen, Jiang Kan, Fu Qi-hua, Yan Li-xing

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 16185534

Genes

RHD

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Related research

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[Serological and molecular study of RHD weak D expression mutant--a case report].PMID 16185534Read ↗

Weak D antigen expression caused by a novel RHD allele in Argentineans.Semantic proximity Read ↗

[A weak D type 59 case identified in the Chinese Han population].Semantic proximity Read ↗

[Molecular genetic analysis of a weak D phenotype].Semantic proximity Read ↗

It's time to phase out "serologic weak D phenotype" and resolve D types with RHD genotyping including weak D type 4.Semantic proximity Read ↗

Molecular characterization of 13 new RHD alleles.Semantic proximity Read ↗

Identification of four novel RHD alleles by weakened antigen D expression.Semantic proximity Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

D-- phenotype caused by a novel RHCE null allele.Semantic proximity Read ↗

Serologic and molecular characterization of weak D type 29.Semantic proximity Read ↗

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman.Semantic proximity Read ↗

Identification of four novel RHD alleles with altered expression of D in Brazilians.Semantic proximity Read ↗

New RhD(IVb) identified in Japanese.Semantic proximity Read ↗

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