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Year | Number of Results |
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2006 | 1 |
2008 | 1 |
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Selection criteria for genetic assessment of patients with familial melanoma.
J Am Acad Dermatol. 2009 Oct;61(4):677.e1-14. doi: 10.1016/j.jaad.2009.03.016.
J Am Acad Dermatol. 2009.
PMID: 19751883
Free PMC article.
Review.
Mutation of the tumour suppressor p33ING1b is rare in melanoma.
Stark M, Puig-Butille JA, Walker G, Badenas C, Malvehy J, Hayward N, Puig S.
Stark M, et al.
Br J Dermatol. 2006 Jul;155(1):94-9. doi: 10.1111/j.1365-2133.2006.07274.x.
Br J Dermatol. 2006.
PMID: 16792758
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Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family.
Maubec E, Chaudru V, Mohamdi H, Blondel C, Margaritte-Jeannin P, Forget S, Corda E, Boitier F, Dalle S, Vabres P, Perrot JL, Lyonnet DS, Zattara H, Mansard S, Grange F, Leccia MT, Vincent-Fetita L, Martin L, Crickx B, Joly P, Thomas L; French Familial Melanoma Study Group; Bressac-de Paillerets B, Avril MF, Demenais F.
Maubec E, et al.
J Am Acad Dermatol. 2012 Dec;67(6):1257-64. doi: 10.1016/j.jaad.2012.05.014. Epub 2012 Jul 26.
J Am Acad Dermatol. 2012.
PMID: 22841127
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A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL).
Harland M, Goldstein AM, Kukalizch K, Taylor C, Hogg D, Puig S, Badenas C, Gruis N, ter Huurne J, Bergman W, Hayward NK, Stark M, Tsao H, Tucker MA, Landi MT, Scarra GB, Ghiorzo P, Kanetsky PA, Elder D, Mann GJ, Holland EA, Bishop DT, Bishop JN; GenoMEL, the Melanoma Genetics Consortium.
Harland M, et al.
Eur J Cancer. 2008 Jun;44(9):1269-74. doi: 10.1016/j.ejca.2008.03.005. Epub 2008 Apr 3.
Eur J Cancer. 2008.
PMID: 18394881
Free PMC article.
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