(Q33370646)

2

1 reference

26 July 2017

Srdjan Novakovic

3

1 reference

26 July 2017

Janez Zgajnar

4

1 reference

26 July 2017

Nikola Besic

5

1 reference

26 July 2017

Marko Hocevar

https://scigraph.springernature.com/pub.10.1186/1471-2350-9-86

6

1 reference

26 July 2017

19 September 2008

1 reference

26 July 2017

1 reference

26 July 2017

9

1 reference

26 July 2017

86

1 reference

26 July 2017

0 references

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Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours.

21 June 2018

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A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation

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21 June 2018

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1 reference

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21 June 2018

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21 June 2018

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A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families

21 June 2018

1 reference

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Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma

21 June 2018

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High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL

21 January 2018

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CDKN2A and CDK4 variants in Latvian melanoma patients: analysis of a clinic-based population

21 January 2018

1 reference

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Genotype-Phenotype Relationships in U.S. Melanoma-Prone Families With CDKN2A and CDK4 Mutations

21 January 2018

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Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

21 January 2018

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Mutation analysis of theCDKN2A promoter in Australian melanoma families

21 January 2018

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Assessment of polymorphic variants in the melanocortin-1 receptor gene with cutaneous pigmentation using an evolutionary approach.

21 January 2018

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A novel L94Q mutation in the CDKN2A gene in a melanoma kindred

31 October 2018

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Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color

21 January 2018

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The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma

21 January 2018

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12 December 2020

MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk

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12 December 2020

The CDKN2a common variants: 148 Ala/Thr and 500 C/G in 3' UTR, and their association with clinical course of melanoma

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12 December 2020

Germline CDKN2A/p16 mutations are rare in multiple primary and familial malignant melanoma in German patients

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12 December 2020

A single nucleotide polymorphism in the 3?untranslated region of theCDKN2A gene is common in sporadic primary melanomas but mutations in theCDKN2B,CDKN2C,CDK4 andp53 genes are rare

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12 December 2020

Analysis of mutations in the p16/CDKN2A gene in sporadic and familial melanoma in the Polish population

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12 December 2020

Germline CDKN2A mutations in childhood melanoma

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12 December 2020

CDKN2A mutations in multiple primary melanomas

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12 December 2020

Population-Based Prevalence of CDKN2A Mutations in Utah Melanoma Families

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