Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2)-Reference-Cited by-同舟云学术

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Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2)

Published:2021-11 Issue: Volume:258-259 Page:101-109
ISSN:2210-7762
Container-title:Cancer Genetics
language:en
Short-container-title:Cancer Genetics

Author:

McReynolds Lisa J.,Biswas Kajal,Giri Neelam,Sharan Shyam K.,Alter Blanche P.

Funder

Division of Cancer Epidemiology and Genetics, National Cancer Institute

National Cancer Institute

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference58 articles.

1. Chromosome instability syndromes;Taylor;Nat Rev Dis Prim,2019

2. Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up;Alter;Haematologica,2018

3. The genomics of inherited bone marrow failure: from mechanism to the clinic;Wegman-Ostrosky;Br J Haematol,2017

4. Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis;Alter;Breast Cancer Res Treat,2020

5. Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2;Alter;J Med Genet,2007

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4. Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study;Journal of Hematology & Oncology;2024-04-29

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