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Results: 1-12 |
Results: 12
HAPLOTYPE ANALYSIS OF 2 RECURRENT CDKN2A MUTATIONS IN 10 MELANOMA FAMILIES - EVIDENCE FOR COMMON FOUNDERS AND INDEPENDENT MUTATIONS
Authors: POLLOCK PM SPURR N BISHOP T NEWTONBISHOP J GRUIS N VANDERVELDEN PA GOLDSTEIN AM TUCKER MA FOULKES WD BARNHILL R HABER D FOUNTAIN J HAYWARD NK
Citation: Pm. Pollock et al., HAPLOTYPE ANALYSIS OF 2 RECURRENT CDKN2A MUTATIONS IN 10 MELANOMA FAMILIES - EVIDENCE FOR COMMON FOUNDERS AND INDEPENDENT MUTATIONS, Human mutation, 11(6), 1998, pp. 424-431
GENETICS OF FAMILIAL ATYPICAL MULTIPLE MOLE-MELANOMA (FAMMM) SYNDROMEIN THE NETHERLANDS - HOW FAR HAVE WE COME
Authors: GRUIS NA VANDERVELDEN PA BERGMAN W FRANTS RR
Citation: Na. Gruis et al., GENETICS OF FAMILIAL ATYPICAL MULTIPLE MOLE-MELANOMA (FAMMM) SYNDROMEIN THE NETHERLANDS - HOW FAR HAVE WE COME, Bulletin du cancer, 85(7), 1998, pp. 627-630
MELANOCORTIN-1 RECEPTOR (MC1R) VARIANT ARG151CYS IS GENERALLY ASSOCIATED WITH FAIR SKIN AND MODIFIES MELANOMA RISK IN DUTCH FAMILIAR ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM)
Authors: GRUIS NA VANDERVELDEN PA SANDKUIJL LA BERGMAN W FRANTS RR
Citation: Na. Gruis et al., MELANOCORTIN-1 RECEPTOR (MC1R) VARIANT ARG151CYS IS GENERALLY ASSOCIATED WITH FAIR SKIN AND MODIFIES MELANOMA RISK IN DUTCH FAMILIAR ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM), American journal of human genetics, 61(4), 1997, pp. 1153-1153
USE OF THE DIRECT RNA AMPLIFICATION TECHNIQUE NASBA TO DETECT FACTOR-V LEIDEN, A POINT MUTATION ASSOCIATED WITH APC RESISTANCE
Authors: REITSMA PH VANDERVELDEN PA VOGELS E VANSTRIJP D TACKEN N ADRIAANSEN H VANGEMEN B
Citation: Ph. Reitsma et al., USE OF THE DIRECT RNA AMPLIFICATION TECHNIQUE NASBA TO DETECT FACTOR-V LEIDEN, A POINT MUTATION ASSOCIATED WITH APC RESISTANCE, Blood coagulation & fibrinolysis, 7(6), 1996, pp. 659-663
HOMOZYGOTES FOR CDKN2 (P16) GERMLINE MUTATION IN DUTCH FAMILIAL MELANOMA KINDREDS
Authors: GRUIS NA VANDERVELDEN PA SANDKUIJL LA PRINS DE WEAVERFELDHAUS J KAMB A BERGMAN W FRANTS RR
Citation: Na. Gruis et al., HOMOZYGOTES FOR CDKN2 (P16) GERMLINE MUTATION IN DUTCH FAMILIAL MELANOMA KINDREDS, Nature genetics, 10(3), 1995, pp. 351-353
CDKN2 EXPLAINS PART OF THE CLINICAL PHENOTYPE IN DUTCH FAMILIAL ATYPICAL MULTIPLE-MOLE MELANOMA (FAMMM) SYNDROME FAMILIES
Authors: GRUIS NA SANDKUIJL LA VANDERVELDEN PA BERGMAN W FRANTS RR
Citation: Na. Gruis et al., CDKN2 EXPLAINS PART OF THE CLINICAL PHENOTYPE IN DUTCH FAMILIAL ATYPICAL MULTIPLE-MOLE MELANOMA (FAMMM) SYNDROME FAMILIES, Melanoma research, 5(3), 1995, pp. 169-177
HOMOZYGOTES FOR CDKN2 P16 GERMLINE MUTATION IN DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM) SYNDROME FAMILIES ARE VIABLE/
Authors: GRUIS NA VANDERVELDEN PA SANDKUIJL LA PRINS DE BERGMAN W FRANTS RR VERMEER BJ
Citation: Na. Gruis et al., HOMOZYGOTES FOR CDKN2 P16 GERMLINE MUTATION IN DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM) SYNDROME FAMILIES ARE VIABLE/, Journal of investigative dermatology, 104(4), 1995, pp. 584-584
VIABILITY OF HOMOZYGOTES FOR A GERMLINE DELETION OF 19 BP IN THE CODING REGION OF THE CDKN2 P16 GENE IN DUTCH MELANOMA FAMILIES/
Authors: FRANTS RR VANDERVELDEN PA SANDKUIJL LA PRINS DE BERGMAN W GRUIS NA
Citation: Rr. Frants et al., VIABILITY OF HOMOZYGOTES FOR A GERMLINE DELETION OF 19 BP IN THE CODING REGION OF THE CDKN2 P16 GENE IN DUTCH MELANOMA FAMILIES/, American journal of human genetics, 57(4), 1995, pp. 338-338
FACTOR-VII AND FIBRINOGEN LEVELS AS RISK-FACTORS FOR VENOUS THROMBOSIS - A CASE-CONTROL STUDY OF PLASMA-LEVELS AND DNA POLYMORPHISMS - THE LEIDEN THROMBOPHILIA STUDY (LETS)
Authors: KOSTER T ROSENDAAL FR REITSMA PH VANDERVELDEN PA BRIET E VANDENBROUCKE JP
Citation: T. Koster et al., FACTOR-VII AND FIBRINOGEN LEVELS AS RISK-FACTORS FOR VENOUS THROMBOSIS - A CASE-CONTROL STUDY OF PLASMA-LEVELS AND DNA POLYMORPHISMS - THE LEIDEN THROMBOPHILIA STUDY (LETS), Thrombosis and haemostasis, 71(6), 1994, pp. 719-722
MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C
Authors: BERTINA RM KOELEMAN BPC KOSTER T ROSENDAAL FR DIRVEN RJ DERONDE H VANDERVELDEN PA REITSMA PH
Citation: Rm. Bertina et al., MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C, Nature, 369(6475), 1994, pp. 64-67
AMINO-ACID DIMORPHISM IN IL1A IS DETECTABLE BY PCR AMPLIFICATION
Authors: VANDERVELDEN PA REITSMA PH
Citation: Pa. Vandervelden et Ph. Reitsma, AMINO-ACID DIMORPHISM IN IL1A IS DETECTABLE BY PCR AMPLIFICATION, Human molecular genetics, 2(10), 1993, pp. 1753-1753
INSTABILITY OF REPEATS OF THE VON-WILLEBRAND FACTOR GENE VARIABLE NUMBER TANDEM REPEAT SEQUENCE IN INTRON-40
Authors: EIKENBOOM JCJ REITSMA PH VANDERVELDEN PA BRIET E
Citation: Jcj. Eikenboom et al., INSTABILITY OF REPEATS OF THE VON-WILLEBRAND FACTOR GENE VARIABLE NUMBER TANDEM REPEAT SEQUENCE IN INTRON-40, British Journal of Haematology, 84(3), 1993, pp. 533-535
Risultati: 1-12 |