AAAAAA

   
Results: 1-25 | 26-32
Results: 1-25/32
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
HB GODAVARI [ALPHA-95(G2)PRO-]THR] - A NEUTRAL AMINO-ACID SUBSTITUTION IN THE ALPHA-1-BETA-2 INTERFACE THAT MODIFIES THE ELECTROPHORETIC MOBILITY OF HEMOGLOBIN
Authors: WAJCMAN H KISTER J RIOU J GALACTEROS F GIROT R MAIERREDELSPERGER M NAYUDU NVS GIORDANO PC
Citation: H. Wajcman et al., HB GODAVARI [ALPHA-95(G2)PRO-]THR] - A NEUTRAL AMINO-ACID SUBSTITUTION IN THE ALPHA-1-BETA-2 INTERFACE THAT MODIFIES THE ELECTROPHORETIC MOBILITY OF HEMOGLOBIN, Hemoglobin, 22(1), 1998, pp. 11-22
THE QUALITY OF ADOLESCENT FRIENDSHIPS - LONG-TERM EFFECTS
Authors: GIORDANO PC CERNKOVICH SA GROAT HT PUGH MD SWINFORD SP
Citation: Pc. Giordano et al., THE QUALITY OF ADOLESCENT FRIENDSHIPS - LONG-TERM EFFECTS, Journal of health and social behavior, 39(1), 1998, pp. 55-71
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
THE INVOLVEMENT OF ALU REPEATS IN RECOMBINATION EVENTS AT THE ALPHA-GLOBIN GENE-CLUSTER - CHARACTERIZATION OF 2 ALPHA(O)-THALASSEMIA DELETION BREAKPOINTS
Authors: HARTEVELD KL LOSEKOOT M FODDE R GIORDANO PC BERNINI LF
Citation: Kl. Harteveld et al., THE INVOLVEMENT OF ALU REPEATS IN RECOMBINATION EVENTS AT THE ALPHA-GLOBIN GENE-CLUSTER - CHARACTERIZATION OF 2 ALPHA(O)-THALASSEMIA DELETION BREAKPOINTS, Human genetics, 99(4), 1997, pp. 528-534
ALPHA-THALASSEMIA IN THE NETHERLANDS - A HETEROGENEOUS SPECTRUM OF BOTH DELETIONS AND POINT MUTATIONS
Authors: HARTEVELD KL LOSEKOOT M HEISTER AJGAM VANDERWIELEN M GIORDANO PC BERNINI LF
Citation: Kl. Harteveld et al., ALPHA-THALASSEMIA IN THE NETHERLANDS - A HETEROGENEOUS SPECTRUM OF BOTH DELETIONS AND POINT MUTATIONS, Human genetics, 100(3-4), 1997, pp. 465-471
THE DISAPPEARANCE OF FETAL AND DONOR RED-BLOOD-CELLS IN ALLOIMMUNIZEDPREGNANCIES - A REAPPRAISAL
Authors: EGBERTS J VANKAMP IL KANHAI HHH MEERMAN RH GIORDANO PC GRAVENHORST JB
Citation: J. Egberts et al., THE DISAPPEARANCE OF FETAL AND DONOR RED-BLOOD-CELLS IN ALLOIMMUNIZEDPREGNANCIES - A REAPPRAISAL, British journal of obstetrics and gynaecology, 104(7), 1997, pp. 818-824
ATTITUDES TOWARD CHILDBEARING AMONG YOUNG PARENTS
Authors: GROAT HT GIORDANO PC CERNKOVICH SA PUGH MD
Citation: Ht. Groat et al., ATTITUDES TOWARD CHILDBEARING AMONG YOUNG PARENTS, Journal of marriage and the family, 59(3), 1997, pp. 568-581
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
HB NYKERK - A NEW DE-NOVO MUTATION AT CODONS-138 139 OF THE BETA-GLOBULIN GENE INDUCING SEVERE HEMOLYTIC-ANEMIA IN A DUTCH GIRL/
Authors: VANDENBERG HM BRUIN MCA HARTEVELD CL VANZWIETEN R GIORDANO PC
Citation: Hm. Vandenberg et al., HB NYKERK - A NEW DE-NOVO MUTATION AT CODONS-138 139 OF THE BETA-GLOBULIN GENE INDUCING SEVERE HEMOLYTIC-ANEMIA IN A DUTCH GIRL/, Blood, 90(10), 1997, pp. 554-554
RAPID DETECTION OF POINT MUTATIONS AND POLYMORPHISMS OF THE ALPHA-GLOBIN GENES BY DGGE AND SSCA HUM MUTAT (VOL 7, PG 114, 1996)
Authors: HARTEVELD KL HEISTER AJGAM GIORDANO PC LOSEKOOT M BERNINI LF
Citation: Kl. Harteveld et al., RAPID DETECTION OF POINT MUTATIONS AND POLYMORPHISMS OF THE ALPHA-GLOBIN GENES BY DGGE AND SSCA HUM MUTAT (VOL 7, PG 114, 1996), Human mutation, 7(4), 1996, pp. 382-382
RAPID DETECTION OF POINT MUTATIONS AND POLYMORPHISMS OF THE ALPHA-GLOBIN GENES BY DGGE AND SSCA
Authors: HARTEVELD KL HEISTER AJGAM GIORDANO PC LOSEKOOT M BERNINI LF
Citation: Kl. Harteveld et al., RAPID DETECTION OF POINT MUTATIONS AND POLYMORPHISMS OF THE ALPHA-GLOBIN GENES BY DGGE AND SSCA, Human mutation, 7(2), 1996, pp. 114-122
HB MALMO [BETA-97(FG-4)HIS-]GLN] LEADING TO POLYCYTHEMIA IN A DUTCH FAMILY
Authors: GIORDANO PC HARTEVELD CL BRAND A WILLEMS LNA KLUINNELEMANS HC PLUG RJ BATELAAN DN BERNINI LF
Citation: Pc. Giordano et al., HB MALMO [BETA-97(FG-4)HIS-]GLN] LEADING TO POLYCYTHEMIA IN A DUTCH FAMILY, Annals of hematology, 73(4), 1996, pp. 183-188
A DUTCH FAMILY WITH HB ATLANTA [BETA-75(E19)LEU-]PRO]
Authors: AYGUN V VANZWIETEN R PRONKADMIRAAL CJ PONJEE GAE DEREGT J HARTEVELD CL GIORDANO PC ROOS D
Citation: V. Aygun et al., A DUTCH FAMILY WITH HB ATLANTA [BETA-75(E19)LEU-]PRO], Hemoglobin, 20(4), 1996, pp. 351-359
HB GOUDA [ALPHA-72(EF1)HIS-]GLN], A NEW SILENT ALPHA-CHAIN VARIANT
Authors: GIORDANO PC HARTEVELD CL KOK PJMJ GEENEN A BATELAAN D AMONS R BERNINI LF
Citation: Pc. Giordano et al., HB GOUDA [ALPHA-72(EF1)HIS-]GLN], A NEW SILENT ALPHA-CHAIN VARIANT, Hemoglobin, 20(1), 1996, pp. 21-29
ADULT, FETAL, AND POLYCYSTIC KIDNEY EXPRESSION OF POLYCYSTIN, THE POLYCYSTIC KIDNEY DISEASE-1 GENE-PRODUCT
Authors: PETERS DJM SPRUIT L KLINGEL R PRINS F BAELDE HJJ GIORDANO PC BERNINI LF DEHEER E BREUNING MH BRUIJN JA
Citation: Djm. Peters et al., ADULT, FETAL, AND POLYCYSTIC KIDNEY EXPRESSION OF POLYCYSTIN, THE POLYCYSTIC KIDNEY DISEASE-1 GENE-PRODUCT, Laboratory investigation, 75(2), 1996, pp. 221-230
MOLECULAR CHARACTERIZATION OF CERATOTOXIN-C, A NOVEL ANTIBACTERIAL FEMALE-SPECIFIC PEPTIDE OF THE CERATOTOXIN FAMILY FROM THE MEDFLY CERATITIS-CAPITATA
Authors: ROSETTO M MANETTI AGO GIORDANO PC MARRI L AMONS R BALDARI CT MARCHINI D DALLAI R
Citation: M. Rosetto et al., MOLECULAR CHARACTERIZATION OF CERATOTOXIN-C, A NOVEL ANTIBACTERIAL FEMALE-SPECIFIC PEPTIDE OF THE CERATOTOXIN FAMILY FROM THE MEDFLY CERATITIS-CAPITATA, European journal of biochemistry, 241(2), 1996, pp. 330-337
AN IVS1-116 (A-]G) ACCEPTOR SPLICE-SITE MUTATION IN THE ALPHA(2) GLOBIN GENE CAUSING ALPHA(+) THALASSEMIA IN 2 DUTCH FAMILIES
Authors: HARTEVELD CL HEISTER JGAM GIORDANO PC BATELAAN D VONDELFT P HAAK HL
Citation: Cl. Harteveld et al., AN IVS1-116 (A-]G) ACCEPTOR SPLICE-SITE MUTATION IN THE ALPHA(2) GLOBIN GENE CAUSING ALPHA(+) THALASSEMIA IN 2 DUTCH FAMILIES, British Journal of Haematology, 95(3), 1996, pp. 461-466
HB UTRECHT [ALPHA(2)129(H12)LEU-]PRO], A NEW UNSTABLE ALPHA-2-CHAIN VARIANT ASSOCIATED WITH A MILD ALPHA-THALASSEMIC PHENOTYPE
Authors: HARTEVELD CL GIORDANO PC LOSEKOOT M HEISTER JGAM VANDELFT DBP BRUIN MCA BERNINI LF
Citation: Cl. Harteveld et al., HB UTRECHT [ALPHA(2)129(H12)LEU-]PRO], A NEW UNSTABLE ALPHA-2-CHAIN VARIANT ASSOCIATED WITH A MILD ALPHA-THALASSEMIC PHENOTYPE, British Journal of Haematology, 94(3), 1996, pp. 483-485
SCHOOL TALK - GENDER AND ADOLESCENT CULTURE - EDER,D, EVANS,CC, PARKER,S
Authors: GIORDANO PC
Citation: Pc. Giordano, SCHOOL TALK - GENDER AND ADOLESCENT CULTURE - EDER,D, EVANS,CC, PARKER,S, American journal of sociology, 102(2), 1996, pp. 640-642
A DE-NOVO DELETION CAUSING EPSILON-GAMMA-DELTA-BETA-THALASSEMIA IN A DUTCH PATIENT
Authors: ABELS J MICHIELS JJ GIORDANO PC BERNINI LF BAYSAL E SMETANINA NS KAZANETZ EG LEONOVA JY HUISMAN THJ
Citation: J. Abels et al., A DE-NOVO DELETION CAUSING EPSILON-GAMMA-DELTA-BETA-THALASSEMIA IN A DUTCH PATIENT, Acta haematologica, 96(2), 1996, pp. 108-109
Risultati: 1-25 | 26-32