A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families (Q34142079)

31 July 2017

title

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

1 reference

Brigitte Bressac-de Paillerets

31 July 2017

author

9

object named as

Bressac-de Paillerets B

1 reference

31 July 2017

Giovanna Bianchi-Scarrà

8

object named as

Bianchi-Scarrà G

2 references

ORCID Public Data File 2021

31 July 2017

Ciotti P

1

1 reference

31 July 2017

Struewing JP

2

1 reference

31 July 2017

Mantelli M

3

1 reference

31 July 2017

Chompret A

4

1 reference

31 July 2017

Avril MF

5

1 reference

31 July 2017

Santi PL

6

1 reference

31 July 2017

Tucker MA

7

1 reference

31 July 2017

Goldstein AM

10

1 reference

31 July 2017

language of work or name

English

0 references

publication date

22 June 2000

1 reference

American Journal of Human Genetics

31 July 2017

published in

1 reference

31 July 2017

volume

67

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31 July 2017

issue

2

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31 July 2017

page(s)

311-319

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CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia.

31 July 2017

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New estimates of intergenerational time intervals for the calculation of age and origins of mutations

5 July 2018

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

5 July 2018

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Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

5 July 2018

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CDKN2 mutations in melanoma

5 July 2018

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

5 July 2018

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Temperature-sensitive mutants of p16CDKN2 associated with familial melanoma

5 July 2018

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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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A genetic history of Italy

5 July 2018

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5 July 2018

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Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations

28 October 2018

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Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution

28 October 2018

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

28 October 2018

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Inhibition of ras-induced proliferation and cellular transformation by p16INK4.

28 October 2018

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Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene

28 October 2018

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Mutations associated with familial melanoma impair p16INK4 function.

28 October 2018

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Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds

28 October 2018

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

28 October 2018

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Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

28 October 2018

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Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

28 October 2018

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Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds

28 October 2018

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12 December 2020

Novel germline p16 mutation in familial malignant melanoma in southern Sweden

1 reference

12 December 2020

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

1 reference

12 December 2020

Germline Mutations of the CDKN2 Gene in UK Melanoma Families

1 reference

12 December 2020

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]

1 reference

12 December 2020

Characterization of ligurian melanoma families and risk of occurrence of other neoplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1086/303001

1 reference

31 July 2017

1 reference

31 July 2017

1 reference