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Results: 1-8 |
Results: 8

Authors: STEENMAN M KRUITBOSCH D WIESMEIJER C ZIJLSTRA N REDEKER E MAGNANI I WESTERVELD A VOUTE P SLATER R MANNENS M
Citation: M. Steenman et al., IDENTIFICATION OF GENES ON CHROMOSOME 1P35-P36 INVOLVED IN THE ETIOLOGY OF SOLID CHILDHOOD TUMORS, European journal of human genetics, 6, 1998, pp. 4142-4142

Authors: KAKORIN S REDEKER E NEUMANN E
Citation: S. Kakorin et al., ELECTROPORATIVE DEFORMATION OF SALT FILLED LIPID VESICLES, European biophysics journal, 27(1), 1998, pp. 43-53

Authors: LOMBARDI MP DEFESCHE JC KAMERLING SWA REDEKER E KASTELEIN JJP HAVEKES LM
Citation: Mp. Lombardi et al., NOVEL MUTATIONS IN THE LDL RECEPTOR GENE OF DUTCH FAMILIAR HYPERCHOLESTEROLEMIC PATIENTS, Atherosclerosis, 130, 1997, pp. 51-51

Authors: REDEKER E DEFESCHE JC LOMBARDI P KASTELEIN JJP MANNENS M
Citation: E. Redeker et al., FREQUENCY AND GEOGRAPHICAL-DISTRIBUTION OF FAMILIAL HYPERCHOLESTEROLEMIA CAUSING MUTATIONS IN THE NETHERLANDS, Atherosclerosis, 130, 1997, pp. 121-121

Authors: STEENMAN M KRUITBOSCH D WIESMEIJER C REDEKER E MAGNANI I WESTERVELD A VOUTE P SLATER R MANNENS M
Citation: M. Steenman et al., IDENTIFICATION OF GENES ON CHROMOSOME 1P35-P36 INVOLVED IN THE ETIOLOGY OF SOLID CHILDHOOD TUMORS, American journal of human genetics, 61(4), 1997, pp. 1416-1416

Authors: REDEKER E ALDERS M HOOVERS JMN RICHARD CW WESTERVELD A MANNENS M
Citation: E. Redeker et al., PHYSICAL MAPPING OF 3 CANDIDATE TUMOR-SUPPRESSOR GENES RELATIVE TO BECKWITH-WIEDEMANN-SYNDROME-ASSOCIATED CHROMOSOMAL BREAKPOINTS AT 11P15.3, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 222-225

Authors: REDEKER E HOOVERS JMN ALDERS M VANMOORSEL CJA IVENS AC GREGORY S KALIKIN L BLIEK J DEGALAN L VANDENBOGAARD R VISSER J VANDERVOORT R FEINBERG AP LITTLE PFR WESTERVELD A MANNENS M
Citation: E. Redeker et al., AN INTEGRATED PHYSICAL MAP OF 210 MARKERS ASSIGNED TO THE SHORT ARM OF HUMAN-CHROMOSOME-11, Genomics, 21(3), 1994, pp. 538-550

Authors: REDEKER E VANMOORSEL CJA FEINBERG A MANNENS M
Citation: E. Redeker et al., TAQI AND RSAI POLYMORPHISMS IN THE H19 GENE (D11S813E), Human molecular genetics, 2(6), 1993, pp. 823-823
Risultati: 1-8 |