(Q57269052)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11477665%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Mutation analysis of the CDKN2A promoter in Australian melanoma families (English)

1 reference

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9 November 2019

0 references

1

1 reference

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9 November 2019

Mitchell S. Stark

2

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9 November 2019

Joanne F Aitken

5

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9 November 2019

Nick Martin

6

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9 November 2019

author name string

Palmer JM

3

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9 November 2019

Walters MK

4

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9 November 2019

Hayward NK

7

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9 November 2019

publication date

1 September 2001

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Genes, Chromosomes and Cancer

9 November 2019

published in

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9 November 2019

volume

32

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9 November 2019

issue

1

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9 November 2019

page(s)

89-94

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Heterogeneity of melanoma risk in families of melanoma patients.

9 November 2019

cites work

1 reference

CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma

21 January 2018

1 reference

Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population

21 January 2018

1 reference

Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds

21 January 2018

1 reference

Regulation of p16CDKN2 expression and its implications for cell immortalization and senescence

21 January 2018

1 reference

Germline p16 mutations in familial melanoma

21 January 2018

1 reference

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus

21 January 2018

1 reference

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma

21 January 2018

1 reference

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]

21 January 2018

1 reference

A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs

21 January 2018

1 reference

CDKN2a/p16INK4a Mutations and Lack of p19ARF Involvement in Familial Melanoma Kindreds

21 January 2018

1 reference

Mutation screening of theCDKN2A promoter in melanoma families

21 January 2018

1 reference

The current situation with regard to human melanoma and genetic inferences.

21 January 2018

1 reference

Increasing incidence of cutaneous melanoma in Queensland, Australia

21 January 2018

1 reference

Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma

21 January 2018

1 reference

Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/GCC.1170

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11477665%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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