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Results:
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Results: 13
Authors:
ONER C
ONER R
BALKAN H
GUMRUK F
GURGEY A
Citation: C. Oner et al., COEXISTENCE OF HB LEPORE-BOSTON-WASHINGTON (DELTA-87GLN-BETA-IVS-II-8) WITH ALPHA-THALASSEMIA [ALPHA(-5NT)ALPHA ALPHA-ALPHA]/, Hemoglobin, 22(3), 1998, pp. 273-276
Authors:
ONER C
ONER R
BIRBEN E
BALKAN H
GUMRUK F
GURGEY A
ALTAY C
Citation: C. Oner et al., HB-H DISEASE WITH HOMOZYGOSITY FOR RED-CELL G6PD DEFICIENCY IN A TURKISH FEMALE, Hemoglobin, 22(2), 1998, pp. 157-160
Authors:
BERKEL AI
BIRBEN E
ONER C
ONER R
YENIAY I
PETRY F
LOOS M
Citation: Ai. Berkel et al., MOLECULAR AND EPIDEMIOLOGIC STUDIES ON SELECTIVE COMPLETE CLQ DEFICIENCY IN TURKEY, Molecular immunology, 35(6-7), 1998, pp. 13-13
Authors:
ALTAY C
ONER C
ONER R
GUMRUK F
MERGEN H
GURGEY A
Citation: C. Altay et al., EFFECT OF ALPHA-GENE NUMBERS ON THE EXPRESSION OF BETA-THALASSEMIA-INTERMEDIA, BETA-THALASSEMIA AND (DELTA-BETA)(0)-THALASSEMIA TRAITS, Human heredity, 48(3), 1998, pp. 121-125
Authors:
ONER C
GURGEY A
ONER R
BALKAN H
GUMRUK F
BAYSAL E
ALTAY C
Citation: C. Oner et al., THE MOLECULAR-BASIS OF HB-H DISEASE IN TURKEY, Hemoglobin, 21(1), 1997, pp. 41-51
Authors:
GURGEY A
BALKAN H
IRKEN G
GUMRUK F
ALTAY S
KALAYCIOGLU A
ONER C
ONER R
Citation: A. Gurgey et al., COMPOUND HETEROZYGOSITY FOR HEMOGLOBIN KNOSSOS [ALPHA(2)BETA(2)-27-(B9)-ALA-SER] AND IVS I-1 MUTATION, Turkish Journal of Pediatrics, 39(2), 1997, pp. 253-257
Authors:
ONER C
ONER R
BALKAN H
GURGEY A
YALCIN A
AVCU F
ALTAY C
Citation: C. Oner et al., MOLECULAR ANALYSIS OF THE TURKISH FORM OF DELETION-INVERSION (DELTA-BETA)CIRCLE THALASSEMIA, British Journal of Haematology, 96(2), 1997, pp. 229-234
Authors:
ALTAY C
ONER C
ONER R
MESCI L
BALKAN H
TUZMEN S
BASAK AN
GUMRUK F
GURGEY A
Citation: C. Altay et al., GENOTYPE-PHENOTYPE ANALYSIS IN HBS-BETA-THALASSEMIA, Human heredity, 47(3), 1997, pp. 161-164
Authors:
SMETANINA NS
ONER CH
BAYSAL E
ONER R
BOZKURT G
ALTAY C
GURGEY A
GU LH
ALTAY C
HUISMAN THJ
Citation: Ns. Smetanina et al., THE RELATIVE LEVELS OF ALPHA(2)-MESSENGER-RNA, ALPHA(1)-MESSENGER-RNA, AND ZETA-MESSENGER-RNA IN HB-H-PATIENTS WITH DIFFERENT DELETIONAL AND NONDELETIONAL ALPHA-THALASSEMIA DETERMINANTS, Biochimica et biophysica acta. Molecular basis of disease, 1316(3), 1996, pp. 176-182
Authors:
ZAREIE MH
ERDEM G
ONER C
ONER R
OGUS A
PISKIN E
Citation: Mh. Zareie et al., INVESTIGATION OF ASCORBATE-CU(II) INDUCED CLEAVAGE OF DNA BY SCANNING-TUNNELING-MICROSCOPY, International journal of biological macromolecules, 19(1), 1996, pp. 69-73
Authors:
ONER R
ONER C
ERDEM G
BALKAN H
OZDAG H
ERKAN M
GUMRUK F
GURGEY A
ALTAY C
Citation: R. Oner et al., A NOVEL (DELTA-BETA)(0)-THALASSEMIA DUE TO A SIMILAR-TO-30-KB DELETION OBSERVED IN A TURKISH FAMILY, Acta haematologica, 96(4), 1996, pp. 232-236
Authors:
ONER C
ONER R
GURGEY A
ALTAY C
Citation: C. Oner et al., A NEW TURKISH TYPE OF BETA-THALASSEMIA-MAJOR WITH HOMOZYGOSITY FOR 2 NON-CONSECUTIVE 7.6-KB DELETIONS OF THE PSI-BETA AND BETA-GENES AND ANINTACT DELTA-GENE, British Journal of Haematology, 89(2), 1995, pp. 306-312
Authors:
DIVOKY V
BAYSAL E
ONER R
CURUK MA
WALKER ELD
INDRAK K
HUISMAN THJ
Citation: V. Divoky et al., THE T-]C MUTATION AT POSITION -GLOBIN GENE IS A RARE POLYMORPHISM THAT DOES NOT CAUSE A BETA-THALASSEMIA AS PREVIOUSLY ASCRIBED(96 OF THE UNTRANSLATED REGION 3' TO THE TERMINATING CODON OF THE BETA), Human genetics, 93(1), 1994, pp. 77-78
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