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The (A)gamma-195 (C -> G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
(Assoc Bras Divulg CientificaSao PauloBrasil, 2001)
MOLECULAR-IDENTIFICATION of HEREDITARY PERSISTENCE of FETAL HEMOGLOBIN TYPE-2 (HPFH TYPE-2) in PATIENTS FROM BRAZIL
(Springer, 1995-03-01)
The HPFH deletion type 2 was first described in a patient from Ghana and is characterized by a large deletion of approximately 105 kb extension. We report here the results obtained in studying a black Brazilian patient who ...
Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
(2011-12-01)
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic conditions, such as hereditary persistence of fetal hemoglobin (HPFH) and delta-beta thalassemia (δβ-thalassemia), Hb F ...
Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
(2011-12-01)
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic conditions, such as hereditary persistence of fetal hemoglobin (HPFH) and delta-beta thalassemia (δβ-thalassemia), Hb F ...
Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster
(Academic Press Inc Elsevier ScienceSan DiegoEUA, 2006)
Simple fluorescent PCR method for detection of large deletions in the beta-globin gene cluster
(Wiley-lissNew YorkEUA, 2003)
MOLECULAR-IDENTIFICATION OF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN TYPE-2 (HPFH TYPE-2) IN PATIENTS FROM BRAZIL
(Springer VerlagNew York, 1995)