Associated Papers
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
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report.
Zareifar S et al.
Bmc Medical Genetics, 2019
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