S.T.O.Saad,
``molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency in Blood donors from Brazil'',
Human Heredity,
47, 17-21,
(1997).
S.T.O.Saad,
``Beta spectrin Campinas: A novel shortened beta chain variant associated with skipping of exon 30 and hereditary elliptocytosis'',
British Journal of Haematology,
79, 579-585,
(1997).
S.T.O.Saad,
``Beta spectrin Campinas: a novel shortened beta chain variant associated with skipping of exon 30 and hereditary elliptocytosis'',
British Journal of Haematology,
79, 579-585,
(1997).
S.T.O.Saad,
``Celula precursora de cordao umbilical humano: Viabilidade para transplantes e terapia genica'',
Revista Brasileira de Clinica e Terapeutica,
23, 127-131,
(1997).
S.T.O.Saad,
``Celula precursora de cordao umbilica humano: Viabilidae para transplnates e terapia genica'',
Revista Brasileira de Clinica e Terapeutica,
23, 127-131,
(1997).
S.T.O.Saad,
``Minimal Doses of Hydroxyurea for Sickle Cell Disease'',
Brazilian Journal of Medical and Biological Research,
30(8), 933-940,
(1997).
S.T.O.Saad,
``Mecanismos de ativação do linfocito T e inducao da leucemia linfoma T do adulto pelo HTLV'',
Revista Brasileira de Clinica e Terapeutica,
23(5), 187-189,
(1997).
S.T.O.Saad,
``Band 3 Campinas: A novel splicing mutation in the Band 3 gene (AE1) associated with hereditary spherocytosis, hyperactivity of Na+/Li+ countertransport and an abnormal renal vicarbonte handling'',
Blood,
90, 2810-2818,
(1997).
S.T.O.Saad,
``Band 3 Campinas: A novel splicing mutation in the Band 3 gene (AE1) associated with hereditary spherocytosis, hyperactivity of Na+/Li+ countertransport and an abnormal renal bicarbonate handling'',
Blood,
90, 2810-2818,
(1997).