451 results on '"Kutlar, F."'
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2. A New Sickling Variant ‘Hb S-Wake β[(Glu6Val-Asn139 Ser)]’ Found in a Compound Heterozygote with Hb S β(Glu6Val) Coinherited with Homozygous α-Thalassemia-2: Phenotype and Molecular Characteristics
3. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, βS-globin gene haplotype, co-inherited α-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia
4. Postmortem molecular diagnosis of sickle β thalassaemia
5. Compound heterozygosity for a β∘-thalassemia (frameshift codons 38/39; -C) and a nondeletional swiss type of HPFH (A→C at NT -110, Gγ) in a Czechoslovakian family
6. One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population
7. The frequency of the γ chain variant AγT in different populations, and its use in evaluating γ gene expression in association with thalassemia
8. DNA polymorphisms in north Sardinian newborns and their linkage with abnormal γ globin gene arrangements and with βo-thalassemia
9. Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya
10. Postmortem molecular diagnosis of sickle beta thalassemia
11. BETA-S HAPLOTYPES IN VARIOUS WORLD POPULATIONS
12. Missense mutation of the last nucleotide of exon 1 (G->C) of globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild allele
13. MOLECULAR CHARACTERIZATION OF BETA-THALASSEMIA IN 174 GREEK PATIENTS WITH THALASSEMIA MAJOR
14. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, betaS-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia
15. Postmortem molecular diagnosis of sickle thalassaemia
16. Frequency of the 677 C?T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients
17. HB Inkster [α85(F6)ASP→VAL] Found in a Caucasian male with Polycythemia
18. An alpha-2 Globin Gene Initiation Codon Mutation in a Vietnamese Patient with Hb H Disease
19. Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1-globin variant, observed in combination with the -(α)20.5 KB α-thal-1 deletion in two Turkish patients
20. New ultra-micro high-performance liquid chromatographic method for determining the γ chain composition of hemoglobin F in normal adults
21. Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients
22. Usefulness of HPLC Methodology for the Characterization of Combinations of the Common β Chain Variants HBS S, C, and O-ARAB, and the α Chain Variant HB G-Philadelphia
23. β-Thalassehia Mutations in the Portuguese; High Frequencies of Two Alleles in Restricted Populations
24. Black β-thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin
25. A NOVEL β°-THALASSAEMIA MUTATION (CODON 15, TGG→TGA) IS PREVALENT IN A POPULATION OF CENTRAL PORTUGAL
26. Molecular characterization of Hb S(C) β‐thalassemia in American blacks
27. The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene [letter]
28. γ Chain Abnormalities and γ-Globin Gene Rearrangements in Newborn Babies of Various Populations
29. A Mild Thalassemia Major Resulting from a Compound Heterozygosity for the IVS-11-1 (G→A) Mutation and the Rare T→C Mutation at the Polyadenylation Site
30. Certain Mutations Observed in the 5´ Sequences of the Gγ- and Aγ-Globin Genes of βs Chromosomes Are Specific for Chromosomes with Major Haplotypes
31. HB Cleveland or α2β293(F9)CYS→ARG;121(GH4)GLU→GLN
32. β-Thalassemia, HB S-β-Thalassemia and Sickle Cell Anemia Among Tunisians
33. Hemoglobinopathies Among the Gond Tribal Groups of Central India; Interaction of α- and β-Thalassemia with β Chain Variants
34. Observations on the levels of Hb A2 in patients with different beta- thalassemia mutations and a delta chain variant
35. Variation in the level of fetal hemoglobin in (δβ)°-thalassemia heterozygotes with different numbers of α-globin genes
36. Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions
37. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, βS-globin gene haplotype, co-inherited α-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
38. Molecular characterization of β‐thalassaemia in 174 Greek patients with thalassaemia major
39. α-Thalassemia DUE toframeshifts at Codons 5, 6, 8, and 8/9; Hematological Observations in Heterozygotes
40. Hb F-Catala or α2gy2l5(A12)Trp →Arg
41. Hb Zengcg or α2β2114(G16)Leu → Met
42. β-Thalassemia in Turkey
43. Hb F-Brooklyn or α2Gγ266(E10)LYSGLN
44. β-Thalassemia in Bulgaria
45. Hb Sun Prae or α213o(H13)Ala → Proβ2A New Unstable Variant Occurring In Low Quantities
46. Compound Heterozygosity for a Mild β+ and a Rare β°-Thalassemia Allele
47. Hb F-Onoda or α2Gγ2146(HC3)Histyr a Newly Discovered Fetal Hemoglobin Variant in a Japanese Newborn
48. Hb F-Jiangsu, The First γ Chain Variant with a Valine -Methionine Substitution: αγ2134(H12) Val→Met
49. Hb F-Charlotte, anAγ Variant with a Threonine Residue in Position γ75 and a Glycine Residue in Position γ136
50. Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.
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