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- 2021
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Mark
Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families
(
- Contribution to journal › Article
- 2019
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Mark
Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma
(
- Contribution to journal › Article
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Mark
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
(
- Contribution to journal › Article
- 2017
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Mark
Rare variant, gene-based association study of hereditary melanoma using whole-exome sequencing
(
- Contribution to journal › Article
- 2016
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Mark
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.
(
- Contribution to journal › Article
- 2015
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Mark
Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma.
(
- Contribution to journal › Article
- 2011
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Mark
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
(
- Contribution to journal › Article
- 2008
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Mark
Common sequence variants on 20q11.22 confer melanoma susceptibility
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- Contribution to journal › Article
- 2007
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Mark
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents
(
- Contribution to journal › Article
- 2006
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Mark
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL
(
- Contribution to journal › Article