Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Counseling and MC1R[original query] |
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Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries. International journal of cancer. Journal international du cancer 2007 Aug 121 (4): 825-31. Goldstein Alisa M, Chaudru Valerie, Ghiorzo Paola, Badenas Celia, Malvehy Josep, Pastorino Lorenza, Laud Karine, Hulley Benjamin, Avril Marie-Francoise, Puig-Butille Joan A, Miniere Annie, Marti Rosa, Chompret Agnes, Cuellar Francisco, Kolm Isabel, Mila Montserrat, Tucker Margaret A, Demenais Florence, Bianchi-Scarra Giovanna, Puig Susana, de-Paillerets Brigitte Bress |
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma. Pigment cell & melanoma research 2008 Dec 21 (6): 700-9. Pastorino L, Bonelli L, Ghiorzo P, Queirolo P, Battistuzzi L, Balleari E, Nasti S, Gargiulo S, Gliori S, Savoia P, Abate Osella S, Bernengo M G, Bianchi Scarrà |
CDKN2a mutation-negative melanoma families have increased risk exclusively for skin cancers but not for other malignancies. International journal of cancer. Journal international du cancer 2015 Nov 137 (9): 2220-6. Helgadottir Hildur, Höiom Veronica, Tuominen Rainer, Jönsson Göran, Månsson-Brahme Eva, Olsson Håkan, Hansson Joh |
NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism. BMC genomics 2022 4 23 (1): 332. Xiao Yuanyuan, Zhou Cong, Xie Hanbing, Huang Shuang, Wang Jing, Liu Shanli |
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