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Results: 1-8 |
Results: 8
A NEWLY DISCOVERED BETA(O)-THALASSEMIA (IVS-II-850, G-]A) MUTATION INA NORTH EUROPEAN FAMILY
Authors: CURUK MA HOWARD SC KUTLAR A HUISMAN THJ
Citation: Ma. Curuk et al., A NEWLY DISCOVERED BETA(O)-THALASSEMIA (IVS-II-850, G-]A) MUTATION INA NORTH EUROPEAN FAMILY, Hemoglobin, 19(3-4), 1995, pp. 207-211
GENETIC-HETEROGENEITY OF BETA-THALASSEMIA IN SOUTHEAST SICILY
Authors: SCHILIRO G DIGREGORIO F SAMPERI P MIRABILE E LIANG R CURUK MA YE Z HUISMAN THJ
Citation: G. Schiliro et al., GENETIC-HETEROGENEITY OF BETA-THALASSEMIA IN SOUTHEAST SICILY, American journal of hematology, 48(1), 1995, pp. 5-11
CORRELATION BETWEEN TRACE-ELEMENTS AND LIPID PROFILES
Authors: YUREGIR GT KAYRIN L CURUK MA ACARTURK E UNLUKURT I
Citation: Gt. Yuregir et al., CORRELATION BETWEEN TRACE-ELEMENTS AND LIPID PROFILES, The Journal of trace elements in experimental medicine, 7(3), 1994, pp. 113-118
BETA-THALASSEMIA ALLELES AND UNSTABLE HEMOGLOBIN TYPES AMONG RUSSIAN PEDIATRIC-PATIENTS
Authors: CURUK MA MOLCHANOVA TP POSTNIKOV YV POBEDIMSKAYA DD LIANG R BAYSAL E KOLODEY S SMETANINA NS TOKAREV YN RUMYANTSEV AG HUISMAN THJ
Citation: Ma. Curuk et al., BETA-THALASSEMIA ALLELES AND UNSTABLE HEMOGLOBIN TYPES AMONG RUSSIAN PEDIATRIC-PATIENTS, American journal of hematology, 46(4), 1994, pp. 329-332
SICKLE-CELL-ANEMIA, SICKLE-CELL BETA-THALASSEMIA, AND THALASSEMIA MAJOR IN ALBANIA - CHARACTERIZATION OF MUTATIONS
Authors: BOLETINI E SVOBODOVA M DIVOKY V BAYSAL E CURUK MA DIMOVSKI AJ LIANG R ADEKILE AD HUISMAN THJ
Citation: E. Boletini et al., SICKLE-CELL-ANEMIA, SICKLE-CELL BETA-THALASSEMIA, AND THALASSEMIA MAJOR IN ALBANIA - CHARACTERIZATION OF MUTATIONS, Human genetics, 93(2), 1994, pp. 182-187
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)
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
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 2 TURKISH PATIENTS
Authors: CURUK MA DIMOVSKI AJ BAYSAL E GU LH KUTLAR F MOLCHANOVA TP WEBBER BB ALTAY C GURGEY A HUISMAN THJ
Citation: Ma. Curuk et al., 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 2 TURKISH PATIENTS, American journal of hematology, 44(4), 1993, pp. 270-275
AN IVS-I-117 (G-]A) ACCEPTOR SPLICE-SITE MUTATION IN THE ALPHA-1-GLOBIN GENE IS A NONDELETIONAL ALPHA-THALASSEMIA-2 DETERMINANT IN AN INDIAN POPULATION
Authors: CURUK MA BAYSAL E GUPTA RB SHARMA S HUISMAN THJ
Citation: Ma. Curuk et al., AN IVS-I-117 (G-]A) ACCEPTOR SPLICE-SITE MUTATION IN THE ALPHA-1-GLOBIN GENE IS A NONDELETIONAL ALPHA-THALASSEMIA-2 DETERMINANT IN AN INDIAN POPULATION, British Journal of Haematology, 85(1), 1993, pp. 148-152
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