Current filters:

Start a new search
Add filters:

Use filters to refine the search results.

Results 1-8 of 8 (Search time: 0.01 seconds).
  • previous
  • 1
  • next
Item hits:
PreviewIssue DateTitleAuthor(s)AdvisorType
2001Apoptotic Cells In A Peripheral Blood Smear In The Context Of Ebv Infection [2]Pagnano K.B.B.; Vassallo J.; Lorand-Metze I.; Costa F.F.; Saad S.T.O.-Carta
2006Hemoglobin Hammersmith [β 42 (cd1) Phe → Ser] In A Brazilian Girl With Congenital Heinz Body Hemolytic Anemia [1]Sonati M.D.F.; Kimura E.M.; Abreu C.F.; Oliveira D.M.; Pinheiro V.R.P.; Costa F.F.-Carta
2008The Deletion Of Sox8 Is Not Associated With Atr-16 In An Hbh Family From BrazilBezerra M.A.C.B.; Araujo A.S.; Phylipsen M.; Balak D.; Kimura E.M.; Oliveira D.M.; Costa F.F.; Sonati M.F.; Harteveld C.L.-Carta
2002Hb Rio Claro Is Caused By A Mutation At The 33rd Position Of The β-globin Chain [β33(b15)val→met] And Not At The 34th PositionCosta F.F.; Sonati M.D.F.-Carta
2002Cmv-dna Detection In Patients With Thrombocytopenia [1]Arruda V.R.; Oliveira G.B.; Annichino-Bizzacchi J.M.; Durante P.; Costa F.F.; Botelho Costa S.C.-Carta
2003Udp-glucuronosyltransferase 1 Gene Promoter Polymorphism Is Associated With Increased Serum Bilirubin Levels And Cholecystectomy In Patients With Sickle Cell Anemia [1]Fertrin K.Y.; Melo M.B.; Assis A.M.; Saad S.T.O.; Costa F.F.-Carta
2000β 0-thalassemia Resulting From A Novel Mutation: β66/u → Stop Codon [4]Grignoli C.R.E.; Carvalho M.H.; Kimura E.M.; Sonati M.F.; Arruda V.R.; Saad S.T.O.; Costa F.F.-Carta
2000Novel Mutation In The Myoc Gene In Primary Open Angle Glaucoma PatientsVasconcellos J.P.C.; Melo M.B.; Costa V.P.; Tsukumo D.M.L.; Basseres D.S.; Bordin S.; Saad S.T.O.; Costa F.F.-Carta