Maria J. Rodrigues

Molecular Defects Underlying the Kell Null Phenotype

Soohee Lee, David Russo, Alexander P. Reiner et al. · Journal of Biological Chemistry · 2001 · 86 citations · Full text

ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O 1v -A 2 hybrid allele that causes four missense mutations in the A transferase

Bahram Hosseini‐Maaf, Åsa Hellberg, Maria J. Rodrigues et al. · BMC Genetics · 2003 · 53 citations · Full text

Identification of six new alleles at the<i>FUT1</i>and<i>FUT2</i>loci in ethnically diverse individuals with Bombay and Para‐Bombay phenotypes

Jill R. Storry, Jannica S. Johannesson, Joyce Poole et al. · Transfusion · 2006 · 44 citations

Weak D type 2 is the most prevalent weak D type in Portugal

Fernando Araújo, Maria J. Rodrigues, Fátima Monteiro et al. · Transfusion Medicine · 2005 · 25 citations

Immunohematology, Weak D., Immunodeficiencies +17

Blood group antigen profile predicted by molecular biology— use of real-time polymerase chain reaction to genotype important <i>KEL</i> , <i>JK</i> , <i>RHD</i> , and <i>RHCE</i> alleles

Fernando Araújo, Cristiana Pereira, Fátima Monteiro et al. · Immunohematology · 2002 · 24 citations