Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography

F. Kutlar, Abdullah Kutlar, T. H. J. Huisman

Journal of Chromatography A

BiochemistryBioanalysisAnalytical ChemistryLiquid ChromatographyClinical Chemistry +5

Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States

J. M. Gonzalez‐Redondo, T. A. Stoming, KD Lanclos, +7

Blood

Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States

J. M. Gonzalez‐Redondo, T. A. Stoming, KD Lanclos, +7

Blood

Fetal hemoglobin in normal adults and ?-thalassemia heterozygotes

Abdullah Kutlar, F. Kutlar, Li-Ghao Gu, +2

Human Genetics

Heme HomeostasisHematologyMaternal HealthMetabolismFetal Hemoglobin +2

A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia

J. M. Gonzalez‐Redondo, T. A. Stoming, Abdullah Kutlar, +7

Blood

Molecular characterization of β‐globin gene mutations in Malay patients with Hb E‐β‐thalassaemia and thalassaemia major

K. G. Yang, F. Kutlar, Elizabeth George, +5

British Journal of Haematology

Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes

JC Diaz-Chico, KG Yang, T. A. Stoming, +5

Blood

Haplotypes of β^SChromosomes Among Patients with Sickle Cell Anemia from Georgia

Y. Hattori, F. Kutlar, Abdullah Kutlar, +2

Hemoglobin

?s Haplotypes in various world populations

Cihan �ner, Aleksandar Dimovski, N F Olivieri, +18

Human Genetics

Allelic VariantHaplotype DeterminationMolecular EcologyMedicineGenetics +7

Pomalidomide augments fetal hemoglobin production without the myelosuppressive effects of hydroxyurea in transgenic sickle cell mice

Steffen E. Meiler, Marlene Wade, F. Kutlar, +6

Blood