(Q38164646)

English

Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

childhood cancer

1 reference

based on heuristic

inferred from title

6

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

object named as

Stefan Meyer

1

0 references

Marc Tischkowitz

2

object named as

Marc Tischkowitz

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

author name string

Kate Chandler

3

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Alan Gillespie

4

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Jillian M Birch

5

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Europe PubMed Central

PubMed publication ID

30 August 2017

language of work or name

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publication date

20 November 2013

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

30 August 2017

51

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Europe PubMed Central

PubMed publication ID

30 August 2017

2

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Europe PubMed Central

PubMed publication ID

30 August 2017

71-75

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Genotype-phenotype correlations in Fanconi anemia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

To the rescue: the Fanconi anemia genome stability pathway salvages replication forks

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathway

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Fanconi anemia and its diagnosis

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

The genetic and molecular basis of Fanconi anemia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Mutation of the RAD51C gene in a Fanconi anemia-like disorder

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Cancer in Fanconi anemia.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Inherited susceptibility to common cancers

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Endocrine abnormalities in patients with Fanconi anemia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Fanconi anemia and biallelic BRCA2 mutation diagnosed in a young child with an embryonal CNS tumor

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Biallelic inactivation of BRCA2 in Fanconi anemia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

X-linked inheritance of Fanconi anemia complementation group B

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Germline Brca2 heterozygosity promotes Kras(G12D) -driven carcinogenesis in a murine model of familial pancreatic cancer

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

The prevalence of BRCA1 and BRCA2 mutations in eastern Chinese women with breast cancer.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

High frequency of recurrent mutations in BRCA1 and BRCA2 genes in Polish families with breast and ovarian cancer.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Common BRCA1 and BRCA2 mutations in breast cancer families: a meta-analysis from systematic review

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Haplotype and cancer risk analysis of two common mutations, BRCA1 4184del4 and BRCA2 2157delG, in high risk northwest England breast/ovarian families

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

High detection rate for BRCA2 mutations in male breast cancer families from North West England

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Should chromosome breakage studies be performed in patients with VACTERL association?

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Childhood cancer in families with and without BRCA1 or BRCA2 mutations ascertained at a high-risk breast cancer clinic

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101642

21 January 2018

Identifiers

10.1136/JMEDGENET-2013-101642

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

ResearchGate publication ID

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