(Q50793851)

19 March 2018

title

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

1 reference

19 March 2018

Gordon Strathdee

12

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Eva Klopocki

object named as

Eva Klopocki

14

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Robert F Wynn

object named as

Robert F Wynn

7

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Anthony D Whetton

object named as

Anthony D Whetton

8

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author name string

Stephanie Smetsers

1

1 reference

19 March 2018

Joanne Muter

2

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19 March 2018

Claire Bristow

3

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19 March 2018

Leena Patel

4

1 reference

19 March 2018

Kate Chandler

5

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19 March 2018

Denise Bonney

6

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19 March 2018

Andrew M Will

9

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19 March 2018

Davy Rockx

10

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19 March 2018

Hans Joenje

11

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19 March 2018

Jonathan Shanks

13

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19 March 2018

Johan J P Gille

15

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19 March 2018

Josephine Dorsman

16

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19 March 2018

Stefan Meyer

17

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19 March 2018

publication date

1 December 2012

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19 March 2018

published in

Familial Cancer

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19 March 2018

volume

11

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19 March 2018

issue

4

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19 March 2018

page(s)

661-665

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19 March 2018

https://scigraph.springernature.com/pub.10.1007/s10689-012-9553-3

exact match

0 references

cites work

The genetic and molecular basis of Fanconi anemia

1 reference

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Mutations of the SLX4 gene in Fanconi anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

Cancer incidence in persons with Fanconi anemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

Fanconi anaemia and leukaemia - clinical and molecular aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

Mutations in BRIP1 confer high risk of ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

Inherited susceptibility to common cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

FANCD2 protein is expressed in proliferating cells of human tissues that are cancer‐prone in Fanconi anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

The NBS1 genetic polymorphisms and the risk of the systemic lupus erythematosus in Taiwanese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-012-9553-3

Genetic subtyping of Fanconi anemia by comprehensive mutation screening

21 January 2018

1 reference

12 December 2020

Defective DNA double-strand break repair in pediatric systemic lupus erythematosus

1 reference

12 December 2020

Genome-wide analysis of genetic alterations in testicular primary seminoma using high resolution single nucleotide polymorphism arrays

1 reference

12 December 2020

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

1 reference

12 December 2020

A heterozygous frameshift mutation in the Fanconi anemia C gene in familial T-ALL and secondary malignancy

1 reference

12 December 2020

10.1007/S10689-012-9553-3

Identifiers

DOI

1 reference

19 March 2018

PubMed ID

22829014

1 reference

19 March 2018