Bergman W - 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. 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

Familial melanoma: a complex disorder leading to controversy on DNA testing.

de Snoo FA, Bergman W, Gruis NA. de Snoo FA, et al. Among authors: bergman w. Fam Cancer. 2003;2(2):109-16. doi: 10.1023/a:1025758527675. Fam Cancer. 2003. PMID: 14574160 Review.

3

From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patients.

de Snoo FA, Kroon MW, Bergman W, ter Huurne JA, Houwing-Duistermaat JJ, van Mourik L, Snels DG, Breuning MH, Willemze R, Frants RR, Gruis NA. de Snoo FA, et al. Among authors: bergman w. J Am Acad Dermatol. 2007 May;56(5):748-52. doi: 10.1016/j.jaad.2007.01.010. Epub 2007 Feb 5. J Am Acad Dermatol. 2007. PMID: 17276542

4

Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.

de Snoo FA, Hottenga JJ, Gillanders EM, Sandkuijl LA, Jones MP, Bergman W, van der Drift C, van Leeuwen I, van Mourik L, Huurne JA, Frants RR, Willemze R, Breuning MH, Trent JM, Gruis NA. de Snoo FA, et al. Among authors: bergman w. Eur J Hum Genet. 2008 Sep;16(9):1135-41. doi: 10.1038/ejhg.2008.72. Epub 2008 Apr 9. Eur J Hum Genet. 2008. PMID: 18398432

5

The absence of multiple atypical nevi in germline CDKN2A mutations: Comment on "Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome".

Ipenburg NA, Gruis NA, Bergman W, van Kester MS. Ipenburg NA, et al. Among authors: bergman w. J Am Acad Dermatol. 2016 Oct;75(4):e157. doi: 10.1016/j.jaad.2016.04.069. J Am Acad Dermatol. 2016. PMID: 27646763 No abstract available.

6

Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families.

van Haeringen A, Bergman W, Nelen MR, van der Kooij-Meijs E, Hendrikse I, Wijnen JT, Khan PM, Klasen EC, Frants RR. van Haeringen A, et al. Among authors: bergman w. Genomics. 1989 Jul;5(1):61-4. doi: 10.1016/0888-7543(89)90086-4. Genomics. 1989. PMID: 2504660

7

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. Among authors: bergman w. Melanoma Res. 1995 Jun;5(3):169-77. doi: 10.1097/00008390-199506000-00005. Melanoma Res. 1995. PMID: 7640518

8

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. Among authors: bergman w. Nat Genet. 1995 Jul;10(3):351-3. doi: 10.1038/ng0795-351. Nat Genet. 1995. PMID: 7670475

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

10

Excess cancer mortality in six Dutch pedigrees with the familial atypical multiple mole-melanoma syndrome from 1830 to 1994.

Hille ET, van Duijn E, Gruis NA, Rosendaal FR, Bergman W, Vandenbroucke JP. Hille ET, et al. Among authors: bergman w. J Invest Dermatol. 1998 May;110(5):788-92. doi: 10.1046/j.1523-1747.1998.00185.x. J Invest Dermatol. 1998. PMID: 9579547 Free article.

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