Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.
about
Molecular structures identified in serologically D- samples of an admixed population.A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.
P2860
Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.
description
2012 nî lūn-bûn
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2012年の論文
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name
Small deletions within the RHD ...... g pathophysiologic mechanisms.
@en
Small deletions within the RHD ...... g pathophysiologic mechanisms.
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type
label
Small deletions within the RHD ...... g pathophysiologic mechanisms.
@en
Small deletions within the RHD ...... g pathophysiologic mechanisms.
@nl
prefLabel
Small deletions within the RHD ...... g pathophysiologic mechanisms.
@en
Small deletions within the RHD ...... g pathophysiologic mechanisms.
@nl
P2093
P2860
P1433
P1476
Small deletions within the RHD ...... g pathophysiologic mechanisms.
@en
P2093
Claude Férec
Cédric Le Maréchal
Déborah Jamet
Isabelle Dupont
Jian-Min Chen
Yann Fichou
P2860
P304
P356
10.1111/J.1537-2995.2012.03713.X
P577
2012-05-21T00:00:00Z