G. C. Carrocini

Inheritance of the Bantu/Benin haplotype causes less severe hemolytic and oxidative stress in sickle cell anemia patients treated with hydroxycarbamide

G. B. Gelaleti, Jéssika V Okumura, Danilo G H Silva, 2016, Journal of Human Genetics.

What influences Hb fetal production in adulthood?

G. C. S. Carrocini, C. Bonini-Domingos, P. J. A. Zamaro, 2011, Revista brasileira de hematologia e hemoterapia.

Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia

E. A. de Almeida, L. Torres, C. Bonini-Domingos, 2013, BMC Medical Genetics.

Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil

C. Bonini-Domingos, C. Lobo, V. Pessoa, 2017, Hemoglobin.

XmnI polymorphism frequency in heterozygote beta thalassemia subjects and its relation to Fetal hemoglobin levels

C. Bonini-Domingos, G. C. Carrocini, Isabela Sandrin Chinelato, 2011, Revista brasileira de hematologia e hemoterapia.

Atypical β-S haplotypes: classification and genetic modulation in patients with sickle cell anemia

Jéssika V Okumura, Danilo G H Silva, L. Torres, 2019, Journal of Human Genetics.

Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.

C. Bonini-Domingos, L. S. Ondei, P. J. A. Zamaro, 2011, Genetics and molecular research : GMR.

Atypical β-S haplotypes: classification and genetic modulation in patients with sickle cell anemia

Jéssika V Okumura, L. Torres, E. Belini-Junior, 2019, Journal of Human Genetics.