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Citation: A. Dagbjartsson et al., A POPULATION SURVEY OF PKU IN ICELAND AND A NOVEL MUTATION IN THE PHAGENE, European journal of human genetics, 6, 1998, pp. 4210-4210
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Citation: K. Gronbaek et al., CONCURRENT DISRUPTION OF CELL-CYCLE ASSOCIATED GENES IN MANTLE CELL LYMPHOMA - A GENOTYPIC AND PHENOTYPIC STUDY OF CYCLIN D1, P16, P15, P53AND PRB, Leukemia, 12(8), 1998, pp. 1266-1271
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Citation: Pt. Straten et al., DETECTION AND CHARACTERIZATION OF ALPHA-BETA-T-CELL CLONALITY BY DENATURING GRADIENT GEL-ELECTROPHORESIS (DGGE), BioTechniques, 25(2), 1998, pp. 244-250
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Citation: P. Guldberg et al., DETECTION OF MUTATIONS IN GC-RICH DNA BY BISULFITE DENATURING GRADIENT GEL-ELECTROPHORESIS, Nucleic acids research, 26(6), 1998, pp. 1548-1549
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Citation: Rb. Gasser et al., ANALYSIS OF SEQUENCE HOMOGENIZATION IN RDNA ARRAYS OF HAEMONCHUS-CONTORTUS BY DENATURING GRADIENT GEL-ELECTROPHORESIS, Electrophoresis, 19(14), 1998, pp. 2391-2395
Citation: P. Guldberg et al., ABERRANT PHENYLALANINE METABOLISM IN PHENYLKETONURIA HETEROZYGOTES, Journal of inherited metabolic disease, 21(4), 1998, pp. 365-372
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Citation: Pt. Straten et al., ACTIVATION OF PREEXISTING T-CELL CLONES BY TARGETED INTERLEUKIN-2 THERAPY, Proceedings of the National Academy of Sciences of the United Statesof America, 95(15), 1998, pp. 8785-8790
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Citation: H. Nissen et al., EVALUATION OF A CLINICALLY APPLICABLE MUTATION SCREENING TECHNIQUE FOR GENETIC DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA AND FAMILIAL DEFECTIVE APOLIPOPROTEIN-B, Clinical genetics, 53(6), 1998, pp. 433-439
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Citation: K. Gronbaek et al., SOMATIC FAS MUTATIONS IN NON-HODGKINS-LYMPHOMA - ASSOCIATION WITH EXTRANODAL DISEASE AND AUTOIMMUNITY, Blood, 92(9), 1998, pp. 3018-3024
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Citation: P. Guldberg et al., A EUROPEAN MULTICENTER STUDY OF PHENYLALANINE-HYDROXYLASE DEFICIENCY - CLASSIFICATION OF 105 MUTATIONS AND A GENERAL SYSTEM FOR GENOTYPE-BASED PREDICTION OF METABOLIC PHENOTYPE, American journal of human genetics, 63(1), 1998, pp. 71-79
Authors:
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FISHLER K
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GUTTLER F
Citation: R. Koch et al., THE RELATIONSHIP OF GENOTYPE TO PHENOTYPE IN PHENYLALANINE-HYDROXYLASE DEFICIENCY, Biochemical and molecular medicine, 60(2), 1997, pp. 92-101
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Citation: P. Guldberg et al., SINGLE-STEP DGGE-BASED MUTATION SCANNING OF THE P53 GENE - APPLICATION TO GENETIC DIAGNOSIS OF COLORECTAL-CANCER, Human mutation, 9(4), 1997, pp. 348-355
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Citation: S. Greberplatzer et al., MOLECULAR HETEROGENEITY OF CLASSICAL AND DUARTE GALACTOSEMIA - MUTATION ANALYSIS BY DENATURING GRADIENT GEL-ELECTROPHORESIS, Human mutation, 10(1), 1997, pp. 49-57
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Citation: P. Guldberg et al., A MOLECULAR SURVEY OF PHENYLKETONURIA IN ICELAND - IDENTIFICATION OF A FOUNDING MUTATION AND EVIDENCE OF PREDOMINANT NORSE SETTLEMENT, European journal of human genetics, 5(6), 1997, pp. 376-381
Authors:
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Citation: Rb. Gasser et al., POLYMERASE CHAIN REACTION-LINKED SINGLE-STRAND CONFORMATION POLYMORPHISM OF RIBOSOMAL DNA TO FINGERPRINT PARASITES, Electrophoresis, 18(9), 1997, pp. 1564-1566
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Citation: P. Guldberg et al., LARGE DELETIONS IN THE PHENYLALANINE-HYDROXYLASE GENE AS A CAUSE OF PHENYLKETONURIA IN INDIA, Journal of inherited metabolic disease, 20(6), 1997, pp. 845-846
Authors:
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GULDBERG P
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HORDER M
Citation: H. Nissen et al., DETECTION AND CHARACTERIZATION OF A NOVEL SPLICE MUTATION IN THE LDL RECEPTOR INTRON-12 RESULTING IN 2 DIFFERENT MUTANT MESSENGER-RNA VARIANTS, Atherosclerosis, 128(1), 1997, pp. 75-83
Authors:
GULDBERG P
KIRKIN AF
GRONBAEK K
STRATEN PT
AHRENKIEL V
ZEUTHEN J
Citation: P. Guldberg et al., COMPLETE SCANNING OF THE CDK4 GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS - A NOVEL MISSENSE MUTATION BUT LOW OVERALL FREQUENCY OF MUTATIONS IN SPORADIC METASTATIC MALIGNANT-MELANOMA, International journal of cancer, 72(5), 1997, pp. 780-783
Authors:
NEDERGAARD T
GULDBERG P
RALFKIAER E
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Citation: T. Nedergaard et al., A ONE-STEP DGGE SCANNING METHOD FOR DETECTION OF MUTATIONS IN THE K-RAS, N-RAS, AND H-RAS ONCOGENES - MUTATIONS AT CODON-12, CODON-13 AND CODON-61 ARE RARE IN B-CELL NON-HODGKINS-LYMPHOMA, International journal of cancer, 71(3), 1997, pp. 364-369
Authors:
GULDBERG P
STRATEN PT
BIRCK A
AHRENKIEL V
KIRKIN AF
ZEUTHEN J
Citation: P. Guldberg et al., DISRUPTION OF THE MMAC1 PTEN GENE BY DELETION OR MUTATION IS A FREQUENT EVENT IN MALIGNANT-MELANOMA/, Cancer research, 57(17), 1997, pp. 3660-3663
Authors:
GRONBAEK K
GULDBERG P
NEDERGAARD T
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MOLLER P
HANSEN NE
HOUJENSEN K
ZEUTHEN J
RALFKIAER E
Citation: K. Gronbaek et al., CONCURRENT DISRUPTION OF CELL-CYCLE ASSOCIATED GENES IN AGGRESSIVE VARIANTS OF MANTLE CELL LYMPHOMAS (MCL), Blood, 90(10), 1997, pp. 3897-3897
Authors:
GULDBERG P
MALLMANN R
HENRIKSEN KF
GUTTLER F
Citation: P. Guldberg et al., PHENYLALANINE-HYDROXYLASE DEFICIENCY IN A POPULATION IN GERMANY - MUTATIONAL PROFILE AND 9 NOVEL MUTATIONS, Human mutation, 8(3), 1996, pp. 276-279