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Results: 1-13 |
Results: 13
IDENTIFICATION OF THE CHINESE IVS-II-654 (C-T) B-THALASSEMIA MUTATIONIN AN IMMIGRANT TURKISH FAMILY - MIGRATION OR RECURRENCE
Authors: TADMOURI GO BILENOGLU O KUTLAR F MARKOWITZ RB KUTLAR A BASAK AN
Citation: Go. Tadmouri et al., IDENTIFICATION OF THE CHINESE IVS-II-654 (C-T) B-THALASSEMIA MUTATIONIN AN IMMIGRANT TURKISH FAMILY - MIGRATION OR RECURRENCE, European journal of human genetics, 6, 1998, pp. 3049-3049
PRENATAL-DIAGNOSIS IN IVF PREGNANCIES - AN INDICATION FOR PREIMPLANTATION GENETICS
Authors: BILENOGLU O BASARAN S YUKSEL A BASAK AN
Citation: O. Bilenoglu et al., PRENATAL-DIAGNOSIS IN IVF PREGNANCIES - AN INDICATION FOR PREIMPLANTATION GENETICS, European journal of human genetics, 6, 1998, pp. 4110-4110
HBS BETA(DEL)-THALASSEMIA ASSOCIATED WITH HIGH-LEVELS OF HEMOGLOBINS A(2) AND F IN A TURKISH FAMILY/
Authors: TADMOURI GO YUKSEL L BASAK AN
Citation: Go. Tadmouri et al., HBS BETA(DEL)-THALASSEMIA ASSOCIATED WITH HIGH-LEVELS OF HEMOGLOBINS A(2) AND F IN A TURKISH FAMILY/, American journal of hematology, 59(1), 1998, pp. 83-86
HOMOZYGOUS BETA-THALASSEMIA ASSOCIATED WITH FAMILIAL MEDITERRANEAN FEVER IN A TURKISH PATIENT
Authors: CANATAN D AYDIN YM AKAR N TASTAN H BILENOGLU O BASAK AN OZSANCAK A TEMIMHAN N
Citation: D. Canatan et al., HOMOZYGOUS BETA-THALASSEMIA ASSOCIATED WITH FAMILIAL MEDITERRANEAN FEVER IN A TURKISH PATIENT, British Journal of Haematology, 102(1), 1998, pp. 53-53
RARE BETA-THALASSEMIA MUTATION IVS-II-848 (C-A) FIRST REPORTED IN A TURKISH CYPRIOT FAMILY
Authors: TUZMEN S BASAK AN BAYSAL E
Citation: S. Tuzmen et al., RARE BETA-THALASSEMIA MUTATION IVS-II-848 (C-A) FIRST REPORTED IN A TURKISH CYPRIOT FAMILY, American journal of hematology, 54(4), 1997, pp. 338-339
RARE BETA-THALASSEMIA MUTATION IN A TURKISH PATIENT - FSC-36 37(-T)/
Authors: TADMOURI GO TUZMEN S BASAK AN
Citation: Go. Tadmouri et al., RARE BETA-THALASSEMIA MUTATION IN A TURKISH PATIENT - FSC-36 37(-T)/, Human biology, 69(2), 1997, pp. 263-267
GENOTYPE-PHENOTYPE ANALYSIS IN HBS-BETA-THALASSEMIA
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
FANCONI APLASTIC-ANEMIA ASSOCIATED WITH BETA-THALASSEMIA TRAIT
Authors: ALTAY C GURGEY A BASAK AN TADMOURI GO SCHROEDERKURT T
Citation: C. Altay et al., FANCONI APLASTIC-ANEMIA ASSOCIATED WITH BETA-THALASSEMIA TRAIT, American journal of hematology, 52(3), 1996, pp. 239-240
PRENATAL-DIAGNOSIS OF BETA-THALASSEMIA AND SICKLE-CELL-ANEMIA IN TURKEY
Authors: TUZMEN S TADMOURI GO OZER A BAIG SM OZCELIK H BASARAN S BASAK AN
Citation: S. Tuzmen et al., PRENATAL-DIAGNOSIS OF BETA-THALASSEMIA AND SICKLE-CELL-ANEMIA IN TURKEY, Prenatal diagnosis, 16(3), 1996, pp. 252-258
MOLECULAR-BASIS AND PRENATAL-DIAGNOSIS OF HEMOGLOBINOPATHIES IN TURKEY
Authors: ALTAY C BASAK AN
Citation: C. Altay et An. Basak, MOLECULAR-BASIS AND PRENATAL-DIAGNOSIS OF HEMOGLOBINOPATHIES IN TURKEY, International journal of pediatric hematology/oncology, 2(4), 1995, pp. 283-290
IMERSLUND-GRASBECK-SYNDROME COEXISTING WITH BETA-THALASSEMIA TRAIT
Authors: SAYLI TR BASAK AN GUMRUK F GURGEY A ALTAY C
Citation: Tr. Sayli et al., IMERSLUND-GRASBECK-SYNDROME COEXISTING WITH BETA-THALASSEMIA TRAIT, Pediatric hematology and oncology, 11(2), 1994, pp. 223-225
A NOVEL 13 BP DELETION IN THE 3'UTR OF THE BETA-GLOBIN GENE CAUSES BETA-THALASSEMIA IN A TURKISH PATIENT
Authors: BASAK AN OZER A KIRDAR B AKAR N
Citation: An. Basak et al., A NOVEL 13 BP DELETION IN THE 3'UTR OF THE BETA-GLOBIN GENE CAUSES BETA-THALASSEMIA IN A TURKISH PATIENT, Hemoglobin, 17(6), 1993, pp. 551-555
A NOVEL DELETION IN A TURKISH BETA-THALASSEMIA PATIENT DETECTED BY DGGE AND DIRECT SEQUENCING - FSC-22-24 (-7 BP)
Authors: OZCELIK H BASAK AN TUZMEN S KIRDAR B AKAR N
Citation: H. Ozcelik et al., A NOVEL DELETION IN A TURKISH BETA-THALASSEMIA PATIENT DETECTED BY DGGE AND DIRECT SEQUENCING - FSC-22-24 (-7 BP), Hemoglobin, 17(4), 1993, pp. 387-391
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