Detalhe da pesquisa
1.
Secondary mutation (c.94_95delAG) in a -α3.7 allele associated with Hb H disease in two unrelated African American individuals homozygous for the -α(3.7) deletion (-α3.7/-α3.7T).
Hemoglobin
; 36(1): 103-7, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22187958
2.
Compound heterozygosity for Hb S [ß6(A3)GluâVal] and Hb Kenya (Aγ81Leu-ß86Ala) in a Ugandan woman.
Hemoglobin
; 36(3): 270-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22384817
3.
New and known ß-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)GluâGln, GAG>>CAG].
Hemoglobin
; 34(5): 445-50, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20854118
4.
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
Nat Genet
; 43(4): 295-301, 2011 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21423179
5.
Interference of hemoglobin Hope on ß-thalassemia: diagnosis by the capillary electrophoresis method.
Am J Clin Pathol
; 137(3): 499-500, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22338067