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Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Universidade Estadual Paulista (Unesp) (1992-07-02)

In order to investigate the effect of folate depletion, lymphocyte sister-chromatid exchange (SCE) rates were compared among homozygous β-thalassaemic patients with low folic acid levels, heterozygous β-thalassaemic patients ...

Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Universidade Estadual Paulista (Unesp) (1992-07-02)

Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Silva, A. E.; Manzato, A. J.; Varella-Garcia, M. (2014)

Thalassemia Intermedia As A Result Of Heterozygosis For β0-thalassemia And αααanti-3.7/αα Genotype In A Brazilian Patient

Kimura E.M.; Grignoli C.R.E.; Pinheiro V.R.P.; Costa F.F.; Sonati M.F. (, 2003)

Mild Clinical Expression Of S-β Thalassemia In A Brazilian Patient With The β+ Ivs-i-6 (t→c) Mutation

De Sonati M.F.; Kaeda J.; Kimura E.M.; Costa F.F.; Luzzatto L. (Brazilian Journal of Genetics, 1998)

Hb Florida: A Novel Elongated C-terminal β-globin Variant Causing Dominant β-thalassemia Phenotype

Weinstein B.I.; Erramouspe B.; Albuquerque D.M.; Oliveira D.M.; Kimura E.M.; Costa F.F.; Sonati M.F. (, 2006)

Two New Unstable Haemoglobins Leading To Chronic Haemolytic Anaemia: Hb Caruaru [β122 (gh5) Phe→ser], A Probable Case Of Germ Line Mutation, And Hb Olinda [β22 (b4) - 25 (b7)], A Deletion Of A 12 Base-pair Sequence

Bezerra M.A.C.; Albuquerque D.M.; Santos M.N.N.; Kimura E.M.; Jorge S.E.D.C.; Oliveira D.M.; Domingues B.L.T.B.; Peres J.C.; Araujo A.S.; Costa F.F.; Sonati M.F. (, 2009)

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Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Thalassemia Intermedia As A Result Of Heterozygosis For β0-thalassemia And αααanti-3.7/αα Genotype In A Brazilian Patient

Mild Clinical Expression Of S-β Thalassemia In A Brazilian Patient With The β+ Ivs-i-6 (t→c) Mutation

Hb Florida: A Novel Elongated C-terminal β-globin Variant Causing Dominant β-thalassemia Phenotype

Two New Unstable Haemoglobins Leading To Chronic Haemolytic Anaemia: Hb Caruaru [β122 (gh5) Phe→ser], A Probable Case Of Germ Line Mutation, And Hb Olinda [β22 (b4) - 25 (b7)], A Deletion Of A 12 Base-pair Sequence

Thalassemia Major Phenotypes Secondary To The Association Of β 5′utr +20(c→t) Allele With β 39(c→t)

Genetic Analysis Of β-thalassemia Major And β-thalassemia Intermedia In Brazil

Identification Of β Thalassemia Mutations In South Brazilians

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Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

Thalassemia Intermedia As A Result Of Heterozygosis For β0-thalassemia And αααanti-3.7/αα Genotype In A Brazilian Patient

Mild Clinical Expression Of S-β Thalassemia In A Brazilian Patient With The β+ Ivs-i-6 (t→c) Mutation

Hb Florida: A Novel Elongated C-terminal β-globin Variant Causing Dominant β-thalassemia Phenotype

Two New Unstable Haemoglobins Leading To Chronic Haemolytic Anaemia: Hb Caruaru [β122 (gh5) Phe→ser], A Probable Case Of Germ Line Mutation, And Hb Olinda [β22 (b4) - 25 (b7)], A Deletion Of A 12 Base-pair Sequence

Thalassemia Major Phenotypes Secondary To The Association Of β 5′utr +20(c→t) Allele With β 39(c→t)

Genetic Analysis Of β-thalassemia Major And β-thalassemia Intermedia In Brazil

Identification Of β Thalassemia Mutations In South Brazilians