Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population.
about
Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.Novel intronic RHD variants identified in serologically D-negative blood donors.Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
P2860
Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
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name
Weak D phenotypes caused by in ...... ied in the Chinese population.
@en
Weak D phenotypes caused by in ...... ied in the Chinese population.
@nl
type
label
Weak D phenotypes caused by in ...... ied in the Chinese population.
@en
Weak D phenotypes caused by in ...... ied in the Chinese population.
@nl
prefLabel
Weak D phenotypes caused by in ...... ied in the Chinese population.
@en
Weak D phenotypes caused by in ...... ied in the Chinese population.
@nl
P2093
P2860
P356
P1433
P1476
Weak D phenotypes caused by in ...... ied in the Chinese population.
@en
P2093
Huanhuan Gao
Zhonghui Guo
P2860
P304
P356
10.1111/TRF.12002
P577
2012-12-07T00:00:00Z