scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0151-9638(06)71042-0 |
P698 | PubMed publication ID | 17072193 |
P50 | author | Julie Charles | Q63987163 |
P2093 | author name string | D Leroux | |
M-T Leccia | |||
I Templier | |||
B Bressac de Paillerets | |||
M-C Combe | |||
P2860 | cites work | Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans | Q24312946 |
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations | Q34020538 | ||
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Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure | Q43073877 | ||
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CDKN2A and MC1R mutations in patients with sporadic multiple primary melanoma | Q47613053 | ||
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Sporadic multiple primary melanoma cases:CDKN2Agermline mutations with a founder effect | Q56893701 | ||
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group [published erratum appears in Hum Mol Genet 1998 May;7(5):941] | Q56893811 | ||
Melanoma and levodopa | Q64891692 | ||
Phaeomelanin versus eumelanin as a chemical indicator of ultraviolet sensitivity in fair-skinned subjects at high risk for melanoma: a pilot study | Q74330411 | ||
Rarity of CDK4 germline mutations in familial melanoma | Q77596261 | ||
P433 | issue | 10 | |
P304 | page(s) | 777-780 | |
P577 | publication date | 2006-10-01 | |
P1433 | published in | Annales de dermatologie et de vénéréologie | Q15767313 |
P1476 | title | [CDKN2A gene mutation and loss of p16 protein activity in a patient on levodopa presenting sporadic multiple primary melanoma] | |
P478 | volume | 133 |