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Results: 1-8 |
Results: 8
THE MOLECULAR-SPECTRUM OF THALASSEMIA AND ABNORMAL-HEMOGLOBINS IN THEDUTCH POPULATION
Authors: GIORDANO PC BERNINI LF HARTEVELD CL HEISTER A BATELAAN D VANDELFT P PLUG R LOSEKOOT M
Citation: Pc. Giordano et al., THE MOLECULAR-SPECTRUM OF THALASSEMIA AND ABNORMAL-HEMOGLOBINS IN THEDUTCH POPULATION, European journal of human genetics, 6, 1998, pp. 3020-3020
A CASE OF NON-BETA-GLOBIN GENE LINKED BETA-THALASSEMIA IN A DUTCH FAMILY WITH 2 ADDITIONAL ALPHA-GENE DEFECTS - THE COMMON -ALPHA(3-CENTER-DOT-7) DELETION AND THE RARE IVS1-116 (A-]G) ACCEPTOR SPLICE-SITE MUTATION
Authors: GIORDANO PC HARTEVELD CL HAAK HL BATELAAN D VANDELFT P PLUG RJ EMONTS M ZANARDINI R BERNINI LF
Citation: Pc. Giordano et al., A CASE OF NON-BETA-GLOBIN GENE LINKED BETA-THALASSEMIA IN A DUTCH FAMILY WITH 2 ADDITIONAL ALPHA-GENE DEFECTS - THE COMMON -ALPHA(3-CENTER-DOT-7) DELETION AND THE RARE IVS1-116 (A-]G) ACCEPTOR SPLICE-SITE MUTATION, British Journal of Haematology, 103(2), 1998, pp. 370-376
BETA-THALASSEMIA, ALPHA-THALASSEMIA AND ABNORMAL-HEMOGLOBINS IN THE ALLOCHTHONOUS AND AUTOCHTHONOUS DUTCH POPULATION
Authors: GIORDANO PC HARTEVELD CL HEISTER JGAM BATELAAN D VANDELFT P PLUG R LOSEKOOT M BERNINI LF
Citation: Pc. Giordano et al., BETA-THALASSEMIA, ALPHA-THALASSEMIA AND ABNORMAL-HEMOGLOBINS IN THE ALLOCHTHONOUS AND AUTOCHTHONOUS DUTCH POPULATION, British Journal of Haematology, 102(1), 1998, pp. 49-49
A NOVEL SPLICE DONOR SITE MUTATION OF THE ALPHA(1)-GLOBIN GENE CAUSING ALPHA-THALASSEMIA
Authors: HARTEVELD CL GIORDANO PC VANDELFT P BATELAAN D BEYER C BERNINI LF
Citation: Cl. Harteveld et al., A NOVEL SPLICE DONOR SITE MUTATION OF THE ALPHA(1)-GLOBIN GENE CAUSING ALPHA-THALASSEMIA, British Journal of Haematology, 102(1), 1998, pp. 50-50
A COMPLEX HEMOGLOBINOPATHY DIAGNOSIS IN A FAMILY WITH BOTH BETA-THALASSEMIA AND ALPHA(0 +)-THALASSEMIA HOMOZYGOSITY/
Authors: GIORDANO PC HARTEVELD CL BOK V VANDELFT P BATELAAN D BRESLAUSIDERIUS EJ BERNINI LF
Citation: Pc. Giordano et al., A COMPLEX HEMOGLOBINOPATHY DIAGNOSIS IN A FAMILY WITH BOTH BETA-THALASSEMIA AND ALPHA(0 +)-THALASSEMIA HOMOZYGOSITY/, British Journal of Haematology, 102(1), 1998, pp. 51-51
GENOTYPE-PHENOTYPE CORRELATION OF DELETION AND NONDELETION ALPHA-THALASSEMIA
Authors: HARTEVELD CL GIORDANO PC ZANARDINI R VANDELFT P BATELAAN D BERNINI LF
Citation: Cl. Harteveld et al., GENOTYPE-PHENOTYPE CORRELATION OF DELETION AND NONDELETION ALPHA-THALASSEMIA, British Journal of Haematology, 102(1), 1998, pp. 52-52
ATYPICAL HBH-DISEASE IN A SURINAMESE PATIENT RESULTING FROM A COMBINATION OF THE -SEA-DELETION AND -ALPHA(3.7)-DELETION WITH HBC HETEROZYGOSITY
Authors: GIORDANO PC HARTEVELD CL MICHIELS JJ TERPSTRA W BATELAAN D VANDELFT P PLUG RJ VANDERWIELEN MJR LOSEKOOT M BERNINI LF
Citation: Pc. Giordano et al., ATYPICAL HBH-DISEASE IN A SURINAMESE PATIENT RESULTING FROM A COMBINATION OF THE -SEA-DELETION AND -ALPHA(3.7)-DELETION WITH HBC HETEROZYGOSITY, British Journal of Haematology, 96(4), 1997, pp. 801-805
HIV-I INFECTION DETECTED BY POLYMERASE CHAIN-REACTION FREQUENTLY PRECEDES ANTIBODY SEROCONVERSION IN DRUG-USERS
Authors: BRUISTEN SM MIENTJES GHC VANDELFT P DEWOLF F VANAMEIJDEN EJC CORNELISSEN M GOUDSMIT J COUTINHO RA HUISMAN JG
Citation: Sm. Bruisten et al., HIV-I INFECTION DETECTED BY POLYMERASE CHAIN-REACTION FREQUENTLY PRECEDES ANTIBODY SEROCONVERSION IN DRUG-USERS, AIDS, 8(12), 1994, pp. 1736-1737
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