Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene (Q72992667)

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31 October 2019

title

Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene (English)

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31 October 2019

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Brigitte Bressac-de Paillerets

10

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Brigitte Bressac-de Paillerets

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31 October 2019

author name string

Gaëlle Bougeard

1

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31 October 2019

Laurence Brugières

2

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31 October 2019

Agnès Chompret

3

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31 October 2019

Paul Gesta

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31 October 2019

Françoise Charbonnier

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31 October 2019

Alexander Valent

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31 October 2019

Cosette Martin

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31 October 2019

Grégory Raux

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31 October 2019

Jean Feunteun

9

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31 October 2019

Thierry Frébourg

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language of work or name

English

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publication date

1 February 2003

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31 October 2019

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31 October 2019

volume

22

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31 October 2019

issue

6

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31 October 2019

page(s)

840-846

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Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206155

7 January 2021

Screening hCHK2 for Mutations

1 reference

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7 January 2021

Linkage studies in a Li-Fraumeni family with increased expression of p53 protein but no germline mutation in p53.

1 reference

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7 January 2021

Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206155

7 January 2021

Identification of a novel PTEN intronic deletion in Li-Fraumeni syndrome and its effect on RNA processing

1 reference

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7 January 2021

Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li-Fraumeni syndrome

1 reference

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7 January 2021

The Li-Fraumeni syndrome

1 reference

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7 January 2021

Sensitivity and predictive value of criteria for p53 germline mutation screening

1 reference

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7 January 2021

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

1 reference

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7 January 2021

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7 January 2021

Absence of germline p16(INK4a) alterations in p53 wild type Li-Fraumeni syndrome families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206155

7 January 2021

Analysis of Li–Fraumeni syndrome and Li–Fraumeni-like families for germline mutations in Bcl10

1 reference

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7 January 2021

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer

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7 January 2021

Li-Fraumeni syndrome – a molecular and clinical review

1 reference

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7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1206155

1 reference

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31 October 2019

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