Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele

RHDvariants in Flanders, Belgium

(2014) Vicky S.T. Van Sandt et al.   TRANSFUSION

Weak D caused by a founder deletion in theRHDgene

(2012) Yann Fichou et al.   TRANSFUSION

RHDandRHCEvariant and zygosity genotyping via multiplex ligation-dependent probe amplification

(2012) Lonneke Haer-Wigman et al.   TRANSFUSION

Establishment of a medium-throughput approach for the genotyping ofRHDvariants and report of nine novel rare alleles

(2012) Yann Fichou et al.   TRANSFUSION

Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles

(2011) Yann Fichou et al.   TRANSFUSION

Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes

(2011) Melina E. Luján Brajovich et al.   TRANSFUSION

Molecular genetics and clinical applications for RH

(2011) Willy A. Flegel   TRANSFUSION AND APHERESIS SCIENCE

RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes

(2011) B. R. Cruz et al.   TRANSFUSION MEDICINE

Phenotype frequencies of blood group systems (Rh, Kell, Kidd, Duffy, MNS, P, Lewis, and Lutheran) in north Indian blood donors

(2010) Beenu Thakral et al.   TRANSFUSION AND APHERESIS SCIENCE

Molecular basis of theRHDgene in blood donors with DEL phenotypes in Shanghai

(2009) Q. Li et al.   VOX SANGUINIS

Frequency of partial D in Western India

(2008) S. Kulkarni et al.   TRANSFUSION MEDICINE