|
Hereditary Melanoma
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma.
|
28592523 |
2017 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Coexisting NRAS and BRAF mutations in primary familial melanomas with specific CDKN2A germline alterations.
|
19759551 |
2010 |
|
Hereditary Melanoma
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Coexisting NRAS and BRAF mutations in primary familial melanomas with specific CDKN2A germline alterations.
|
19759551 |
2010 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
|
Hereditary Melanoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Coexisting NRAS and BRAF mutations in primary familial melanomas with specific CDKN2A germline alterations.
|
19759551 |
2010 |
|
Hereditary Melanoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
|
Hereditary Melanoma
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
CDKN2A germline mutations in individuals with cutaneous malignant melanoma.
|
17218939 |
2007 |
|
Hereditary Melanoma
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
|
16905682 |
2007 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
|
16905682 |
2007 |
|
Hereditary Melanoma
|
|
0.700 |
GeneticVariation
|
CLINVAR |
CDKN2A germline mutations in individuals with cutaneous malignant melanoma.
|
17218939 |
2007 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma: an international population-based study.
|
16896043 |
2006 |
|
Hereditary Melanoma
|
|
0.700 |
GeneticVariation
|
CLINVAR |
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
|
17047042 |
2006 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
|
17047042 |
2006 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample.
|
16234564 |
2005 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Familial melanoma, pancreatic cancer and germline CDKN2A mutations.
|
15146471 |
2004 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Geographical variation in the penetrance of CDKN2A mutations for melanoma.
|
12072543 |
2002 |
|
Hereditary Melanoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations.
|
11500805 |
2001 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Validation of denaturing high performance liquid chromatography as a rapid detection method for the identification of human INK4A gene mutations.
|
11687599 |
2001 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
CDKN2A variants in a population-based sample of Queensland families with melanoma.
|
10070944 |
1999 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
The p16INK4a/CDKN2A tumor suppressor and its relatives.
|
9823374 |
1998 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds.
|
9416844 |
1997 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
CDKN2A (p16INK4A) somatic and germline mutations.
|
8723678 |
1996 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.
|
8595405 |
1995 |
|
Hereditary Melanoma
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.
|
8595405 |
1995 |