Frants RR - Search Results

1

Genetics of seven Dutch familial atypical multiple mole-melanoma syndrome families: a review of linkage results including chromosomes 1 and 9.

Bergman W, Gruis NA, Sandkuijl LA, Frants RR. Bergman W, et al. Among authors: frants rr. J Invest Dermatol. 1994 Nov;103(5 Suppl):122S-125S. doi: 10.1111/1523-1747.ep12399430. J Invest Dermatol. 1994. PMID: 7963673 Free article.

2

Genetic heterogeneity of familial hemiplegic migraine.

Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: frants rr. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770

3

Linkage analysis in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families. Effect of naevus count.

Gruis NA, Sandkuijl LA, Weber JL, van der Zee A, Borgstein AM, Bergman W, Frants RR. Gruis NA, et al. Among authors: frants rr. Melanoma Res. 1993 Aug;3(4):271-7. Melanoma Res. 1993. PMID: 8219760

4

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.

Terwindt GM, Ophoff RA, Lindhout D, Haan J, Halley DJ, Sandkuijl LA, Brouwer OF, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: frants rr. Epilepsia. 1997 Aug;38(8):915-21. doi: 10.1111/j.1528-1157.1997.tb01257.x. Epilepsia. 1997. PMID: 9579893 Free article.

5

Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?

Gruis NA, Van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: frants rr. Bull Cancer. 1998 Jul;85(7):627-30. Bull Cancer. 1998. PMID: 9752270 Free article.

6

A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families.

van der Velden PA, Sandkuijl LA, Bergman W, Hille ET, Frants RR, Gruis NA. van der Velden PA, et al. Among authors: frants rr. Genome Res. 1999 Jun;9(6):575-80. Genome Res. 1999. PMID: 10400925 Free PMC article.

7

Familial melanoma; CDKN2A and beyond.

Gruis NA, van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: frants rr. J Investig Dermatol Symp Proc. 1999 Sep;4(1):50-4. doi: 10.1038/sj.jidsp.5640181. J Investig Dermatol Symp Proc. 1999. PMID: 10537008 Free article. Review.

8

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden).

Vasen HF, Gruis NA, Frants RR, van Der Velden PA, Hille ET, Bergman W. Vasen HF, et al. Among authors: frants rr. Int J Cancer. 2000 Sep 15;87(6):809-11. Int J Cancer. 2000. PMID: 10956390

9

Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.

van der Velden PA, Sandkuijl LA, Bergman W, Pavel S, van Mourik L, Frants RR, Gruis NA. van der Velden PA, et al. Among authors: frants rr. Am J Hum Genet. 2001 Oct;69(4):774-9. doi: 10.1086/323411. Epub 2001 Aug 7. Am J Hum Genet. 2001. PMID: 11500806 Free PMC article.

10

Facioscapulohumeral muscular dystrophy in the Dutch population.

Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. Padberg GW, et al. Among authors: frants rr. Muscle Nerve Suppl. 1995;(2):S81-4. Muscle Nerve Suppl. 1995. PMID: 23573591

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