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Hb Florida: A novel elongated C-terminal beta-globin variant causing dominant beta-thalassemia phenotype
(Wiley-lissHobokenEUA, 2006)
Hb S-Sao Paulo: A new sickling hemoglobin with stable polymers and decreased oxygen affinity
(ElsevierNew York, 2012)
Rastreamento de hemoglobinas variantes e talassemias com associação de métodos de diagnóstico
(2008-01-01)
The neonatal diagnosis hemoglobinopathies improves the quality of life by prophylactic measures and genetic counseling. The diagnosis of variant hemoglobins and thalassemias was considered in the present study. Cord blood ...
A novel beta-globin variant: Hb Pocos de Caldas [beta 61(E5)Lys -> Gln]
(Marcel Dekker IncNew YorkEUA, 2002)
Hb H disease resulting from the association of an alpha(0)-thalassemia allele [-(alpha)(20.5)] with an unstable alpha-globin variant [Hb Icaria]: First report on the occurrence in Brazil
(Soc Brasil GeneticaRibeirao PretBrasil, 2009)
Amplificação gênica alelo-específica na caracterização das hemoglobinas S, C e D e as interações entre elas e talassemias beta
(Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de Citopatologia, 2006-08-01)
INTRODUÇÃO: As hemoglobinopatias resultam de alterações hereditárias, sendo prevalentes em muitas regiões do mundo, mas atingem a população brasileira de forma significativa. Elas são decorrentes de alterações em genes ...
POLYMORPHISM IN THE HMOX1 GENE IS ASSOCIATED WITH HIGH LEVELS OF FETAL HEMOGLOBIN IN BRAZILIAN PATIENTS WITH SICKLE CELL ANEMIA
(Informa HealthcareLondonInglaterra, 2013)