Maria Letícia Ribeiro

Thiamine-Responsive Megaloblastic Anemia: Identification of Novel Compound Heterozygotes and Mutation Update

Anke Bergmann, Inderneel Sahai, Jill Falcone et al. · The Journal of Pediatrics · 2009 · 87 citations · Full text

Laboratory Hematology, Biochemistry, Novel Compound Heterozygotes +12

?s Haplotypes in various world populations

Cihan �ner, Aleksandar Dimovski, N F Olivieri et al. · Human Genetics · 1992 · 84 citations

Allelic Variant, Haplotype Determination, Molecular Ecology +9

Molecular characterization of ?-thalassemia in Azerbaijan

Chingiz Asadov, T. Dadasova, Lihao Gu et al. · Human Genetics · 1992 · 41 citations

Molecular Characterization, Biochemical Taxonomy, Genetics +3

Dominant β‐thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β‐globin gene

R. Öner, C. Öner, J. B. Wilson et al. · British Journal of Haematology · 1991 · 34 citations

β-Thalassehia Mutations in the Portuguese; High Frequencies of Two Alleles in Restricted Populations

G. P. Tamagnini, Paula Gonçalves, Maria Letícia Ribeiro et al. · Hemoglobin · 1993 · 30 citations