(Q57419715)

Ines Zanna

5

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Irene Piaceri

Irene Piaceri

4

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Francesco Sera

Francesco Sera

6

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Laura Papi

Laura Papi

1

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Maurizio Genuardi

Maurizio Genuardi

8

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Domenico Palli

Domenico Palli

9

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author name string

Caterina Congregati

3

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Doralba Morrone

https://scigraph.springernature.com/pub.10.1007/s10689-009-9295-z

7

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publication date

18 September 2009

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published in

Familial Cancer

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volume

9

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issue

2

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page(s)

181-185

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exact match

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cites work

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

1 reference

12 December 2020

A recurrent mutation in PALB2 in Finnish cancer families.

1 reference

12 December 2020

Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women

1 reference

12 December 2020

Analysis of PALB2/FANCN-associated breast cancer families

1 reference

12 December 2020

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

1 reference

12 December 2020

Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families

1 reference

12 December 2020

Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history.

1 reference

12 December 2020

Information analysis of human splice site mutations

1 reference

12 December 2020

PALB2 sequence variants in young South African breast cancer patients

1 reference

12 December 2020

Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2

1 reference

12 December 2020

The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives

1 reference

12 December 2020

Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories?

1 reference

12 December 2020

BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes

1 reference

12 December 2020

Penetrance analysis of the PALB2 c.1592delT founder mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

Automated splicing mutation analysis by information theory.

1 reference

12 December 2020