Gruis NA - Search Results

1

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.

Gruis NA, Sandkuijl LA, van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Melanoma Res. 1995 Jun;5(3):169-77. doi: 10.1097/00008390-199506000-00005. Melanoma Res. 1995. PMID: 7640518

2

The Dutch FAMMM family material: clinical and genetic data.

Bergman W, Gruis NA, Frants RR. Bergman W, et al. Among authors: gruis na. Cytogenet Cell Genet. 1992;59(2-3):161-4. doi: 10.1159/000133232. Cytogenet Cell Genet. 1992. PMID: 1737487 No abstract available.

3

Locus for susceptibility to melanoma on chromosome 1p.

Gruis NA, Bergman W, Frants RR. Gruis NA, et al. N Engl J Med. 1990 Mar 22;322(12):853-4. doi: 10.1056/nejm199003223221217. N Engl J Med. 1990. PMID: 2308622 No abstract available.

4

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds.

Gruis NA, van der Velden PA, Sandkuijl LA, Prins DE, Weaver-Feldhaus J, Kamb A, Bergman W, Frants RR. Gruis NA, et al. Nat Genet. 1995 Jul;10(3):351-3. doi: 10.1038/ng0795-351. Nat Genet. 1995. PMID: 7670475

5

CDKN2 (MTS1) tumor suppressor gene mutations in human tumor cell lines.

Liu Q, Neuhausen S, McClure M, Frye C, Weaver-Feldhaus J, Gruis NA, Eddington K, Allalunis-Turner MJ, Skolnick MH, Fujimura FK, et al. Liu Q, et al. Among authors: gruis na. Oncogene. 1995 Mar 16;10(6):1061-7. Oncogene. 1995. PMID: 7700630

6

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: gruis na. J Invest Dermatol. 1994 Nov;103(5 Suppl):122S-125S. doi: 10.1111/1523-1747.ep12399430. J Invest Dermatol. 1994. PMID: 7963673 Free article.

7

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.

Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis NA, Ding W, Hussey C, Tran T, Miki Y, Weaver-Feldhaus J, et al. Kamb A, et al. Among authors: gruis na. Nat Genet. 1994 Sep;8(1):23-6. doi: 10.1038/ng0994-22. Nat Genet. 1994. PMID: 7987388

8

PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue.

Gruis NA, Abeln EC, Bardoel AF, Devilee P, Frants RR, Cornelisse CJ. Gruis NA, et al. Br J Cancer. 1993 Aug;68(2):308-13. doi: 10.1038/bjc.1993.333. Br J Cancer. 1993. PMID: 8102243 Free PMC article.

9

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. Melanoma Res. 1993 Aug;3(4):271-7. Melanoma Res. 1993. PMID: 8219760

10

Familial melanoma and pancreatic cancer.

Bergman W, Gruis N. Bergman W, et al. N Engl J Med. 1996 Feb 15;334(7):471-2. N Engl J Med. 1996. PMID: 8552160 No abstract available.

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