Carta
Hemoglobin Hammersmith [β 42 (cd1) Phe → Ser] In A Brazilian Girl With Congenital Heinz Body Hemolytic Anemia [1]
Registro en:
Pediatric Blood And Cancer. , v. 47, n. 6, p. 855 - 856, 2006.
15455009
10.1002/pbc.20851
2-s2.0-33749187307
Autor
Sonati M.D.F.
Kimura E.M.
Abreu C.F.
Oliveira D.M.
Pinheiro V.R.P.
Costa F.F.
Institución
Resumen
[No abstract available] 47 6 855 856 Akiyama, M., Murayama, S., Yokoi, K., Hemoglobin Hamersmith [β42 (CD1) Phe-Ser] causing a severe hemolytic anemia in a Japanese girl (2006) Pediatr Blood Cancer, , (e-pub ahead of print) Dacie, J.V., Shinton, N.K., Gaffney, P.J., Haemoglobin Hammersmith [β42 (CD1) Phe-Ser] (1967) Nature, 216, pp. 663-665 Tuohy, A.M., Mckie, V.C., Sabio, H., Hb Hammersmith [β42 (CD1) Phe-Ser]: Occurrence as de novo mutation in black monozygotic twins with multiple congenital anomalies (1998) Pediatr Hematol Oncol, 20, pp. 563-566 (1995) Practical Haematology. 8th Edition, 609p. , Dacie JV, Lewis SM, editors. Edinburgh, Hong Kong, London, Madrid, Melbourne, New York and Tokyo: Churchill Livingstone Miranda, S.R.P., Fonseca, S.F., Figueiredo, M.S., Hb Köln [α2β298(FG5)val-met] identified by DNA analysis in a Brazilian family (1997) Braz J Genet, 20, pp. 745-748 Giusti, A.M., Budiowle, B.A., A chemiluminescence-based detection system for human DNA quantitation and restriction fragment length polymorphism (RFLP) analysis (1995) Appl Theor Electrophor, 5, pp. 89-98