Associated Papers
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis.
Joshi G et al.
Journal of Medical Genetics, 2023
36894310 (PubMed )
Supplement: jmg-2022-108714supp003.pdf
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
George M et al.
Human Mutation, 2021
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-s005.docx
Severe telomere shortening in Fanconi anemia complementation group L.
Shah A et al.
Molecular Biology Reports, 2021
Characterization of two novel FANCG mutations in Indian Fanconi anemia patients.
Solanki A et al.
Leukemia Research, 2017
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