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Biochimica Et Biophysica Acta|August 23, 1996
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinantsN S Smetanina, C Oner, E Baysal, et al.Biochemical and Biophysical Research Communications|June 16, 1988
Beta-thalassemia due to a T----A mutation within the ATA boxY J Fei, T A Stoming, G D Efremov, et al.Blood|January 1, 1988
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probesJ C Diaz-Chico, K G Yang, T A Stoming, et al.British Journal of Haematology|April 1, 1994
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutationD G Efremov, A J Dimovski, E Baysal, et al.Human Genetics|April 1, 1992
Beta S haplotypes in various world populationsC Oner, A J Dimovski, N F Olivieri, et al.Blood|May 1, 1989
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-thalassemiaJ M Gonzalez-Redondo, T A Stoming, A Kutlar, et al.American Journal of Hematology|December 1, 1993
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patientsM A Cürük, A J Dimovski, E Baysal, et al.American Journal of Human Genetics|August 1, 1996
A locus for Fanconi anemia on 16q determined by homozygosity mappingM Gschwend, O Levran, L Kruglyak, et al.Nucleic Acids Research|February 15, 1996
Antisense oligonucleotide containing an internal, non-nucleotide-based linker promote site-specific cleavage of RNAM A Reynolds, T A Beck, P B Say, et al.Clinical Diabetes and Endocrinology|October 1, 2021
Risk factors for diabetic foot ulcers in metreleptin naïve patients with lipodystrophyO Saydam, B Ozgen Saydam, S C Adiyaman, et al.Pageof 16