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Hemoglobin|March 18, 2000
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish familyF Gümrük, H Mergen, R Oner, et al.Hemoglobin|March 18, 2000
A new, electrophoretically silent, fetal hemoglobin variant: Hb F-Calabria [Ggamma118(GH1)Phe-->Leu]L Manca, L Cherchi, M C De Rosa, et al.Hemoglobin|November 24, 1999
Characterization of a new polymorphism, IVS-I-108 (T-->C), and a new beta-thalassemia mutation, -27 (A-->T), discovered in the course of a prenatal diagnosisC Badens, N Jassim, N Martini, et al.Hemoglobin|January 17, 2002
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin geneJ S Waye, B Eng, M Patterson, et al.Hemoglobin|January 17, 2002
A multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reactionJ M Old, S N Khan, I Verma, et al.Hemoglobin|October 31, 2002
Beta-thalassemia intermedia and non-Hodgkin's lymphomaAref Chehal, Rabih Loutfi, Ali TaherHemoglobin|August 2, 2001
The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell diseaseA Kutlar, F Kutlar, I Turker, et al.Hemoglobin|January 1, 1997
Alpha-, beta-, and gamma-mRNA levels in beta-thalassemia; transcriptional and translational differences in heterozygotes, homozygotes, and compound heterozygotesN S Smetanina, L H Gu, L Simjanovska, et al.Hemoglobin|January 1, 1997
The molecular basis of Hb H disease in TurkeyC Oner, A Gürgey, R Oner, et al.Pageof 240