Small deletions within theRHDcoding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms

Weak D caused by a founder deletion in theRHDgene

(2012) Yann Fichou et al.   TRANSFUSION

Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture

(2012) Monique Silvy et al.   TRANSFUSION

On the sequence-directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease

(2011) David N. Cooper et al.   HUMAN MUTATION

Partial D phenotypes and genotypes in the Chinese population

(2011) Luyi Ye 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

Molecular genetics and clinical applications for RH

(2011) Willy A. Flegel   TRANSFUSION AND APHERESIS SCIENCE

Genomic rearrangements in inherited disease and cancer

(2010) Jian-Min Chen et al.   SEMINARS IN CANCER BIOLOGY

RhD variant caused by an in-frame triplet duplication in the RHD gene

(2010) Janet C. Pereira et al.   TRANSFUSION

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

(2010) Monique Silvy et al.   TRANSFUSION

RHCEalleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany

(2009) Andrea Döscher et al.   TRANSFUSION

The Human Gene Mutation Database: 2008 update

(2009) Peter D Stenson et al.   Genome Medicine

Six years' experience performingRHDgenotyping to confirm D− red blood cell units in Germany for preventing anti-D immunizations

(2008) Willy A. Flegel et al.   TRANSFUSION