Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)We describe here two new unstable beta-globin variants, Hb Caruaru and Hb Olinda, found in northeastern Brazil, both associated with chronic haemolytic anaemia. Haemoglobin Caruaru is caused by a single base substitution at codon 122 (TTC -> TCC), possibly originating from the germ line cells of the patient's grandmother. Haemoglobin Olinda is also a de novo mutation, caused by a 12 bp deletion leading to the removal of the 22nd to the 25th residues of the normal beta-globin chain.834378382Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CN...
Two healthy newborns, heterozygous for two different Y-globin chain mutations, were observed during...
Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While s...
Three novel alpha-globin variants were found during a screening program for hemoglobinopathies in bl...
We describe here two new unstable β-globin variants, Hb Caruaru and Hb Olinda, found in northeastern...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
Hb H Disease is caused by the loss or inactivation of three of the four functional α-globin genes. P...
This study describes a new molecular condition in the α2- globin gene (HBA2) found in six unrelated ...
The various clinical phenotypes in beta-thalassemias have stimulated the study of genetic factors th...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
Hemoglobin structural abnormalities are among the most commonly found human genetic diseases. The La...
A patient with Hb H disease resulting from the association of the - α3.7 rightward deletion with the...
International audienceWe report three cases with very heterogeneous Hb A(2) levels caused by known c...
Hemoglobinopathies are the most common autosomal recessive disorders and are mostly inherited in a r...
We report the clinical and laboratory findings concerning three unrelated Brazilian patients investi...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Two healthy newborns, heterozygous for two different Y-globin chain mutations, were observed during...
Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While s...
Three novel alpha-globin variants were found during a screening program for hemoglobinopathies in bl...
We describe here two new unstable β-globin variants, Hb Caruaru and Hb Olinda, found in northeastern...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
Hb H Disease is caused by the loss or inactivation of three of the four functional α-globin genes. P...
This study describes a new molecular condition in the α2- globin gene (HBA2) found in six unrelated ...
The various clinical phenotypes in beta-thalassemias have stimulated the study of genetic factors th...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
Hemoglobin structural abnormalities are among the most commonly found human genetic diseases. The La...
A patient with Hb H disease resulting from the association of the - α3.7 rightward deletion with the...
International audienceWe report three cases with very heterogeneous Hb A(2) levels caused by known c...
Hemoglobinopathies are the most common autosomal recessive disorders and are mostly inherited in a r...
We report the clinical and laboratory findings concerning three unrelated Brazilian patients investi...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Two healthy newborns, heterozygous for two different Y-globin chain mutations, were observed during...
Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While s...
Three novel alpha-globin variants were found during a screening program for hemoglobinopathies in bl...