Authors:
van der Velden, PA
Metzelaar-Blok, JAW
Bergman, W
Hurks, HMH
Frants, RR
Gruis, NA
Jager, MJ
Citation: Pa. Van Der Velden et al., Promoter hypermethylation: A common cause of reduced p16(INK4a) expressionin uveal melanoma, CANCER RES, 61(13), 2001, pp. 5303-5306
Authors:
van der Velden, PA
Sandkuijl, LA
Bergman, W
Pavel, S
van Mourik, L
Frants, RR
Gruis, NA
Citation: Pa. Van Der Velden et al., Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma, AM J HU GEN, 69(4), 2001, pp. 774-779
Authors:
Bastiaens, MT
ter Huurne, JAC
Kielich, C
Gruis, NA
Westendorp, RGJ
Vermeer, BJ
Bavinck, NJB
Citation: Mt. Bastiaens et al., Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair, AM J HU GEN, 68(4), 2001, pp. 884-894
Authors:
Vasen, HFA
Gruis, NA
Frants, RR
van der Velden, PA
Hille, ETM
Bergman, W
Citation: Hfa. Vasen et al., Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden), INT J CANC, 87(6), 2000, pp. 809-811
Authors:
van der Velden, PA
Sandkuijl, LA
Bergman, W
Hille, ETM
Frants, RR
Gruis, NA
Citation: Pa. Van Der Velden et al., A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families, GENOME RES, 9(6), 1999, pp. 575-580
Authors:
Snels, DGCTM
Hille, ETM
Gruis, NA
Bergman, W
Citation: Dgctm. Snels et al., Risk of cutaneous malignant melanoma in patients with nonfamilial atypicalnevi from a pigmented lesions clinic, J AM ACAD D, 40(5), 1999, pp. 686-693