Associated Papers
Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia.
Zagnoli-Vieira G et al.
Human Genetics, 2023
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG.
Reyes P et al.
International Journal of Molecular Sciences, 2022
The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature.
Thompson AS et al.
Molecular Genetics & Genomic Medicine, 2021
33960719 (PubMed )
Supplement: MGG3-9-e1693-s002.docx
Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer.
Zeng B et al.
Frontiers in Oncology, 2021
33889545 (PubMed )
Supplement: Table_11.XLSX › Sheet1
Canonical and Noncanonical Roles of Fanconi Anemia Proteins: Implications in Cancer Predisposition.
Milletti G et al.
Cancers, 2020
Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.
Dillon B et al.
Molecular Genetics & Genomic Medicine, 2020
Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei.
Francies FZ et al.
Dna Repair, 2018
Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.
Feben C et al.
Familial Cancer, 2017
Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patients.
Ghazwani Y et al.
Cancer Genetics, 2016
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