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Frontiers | Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion: A case report
Erin's Cure FA Page - 🤰 INHERITANCE 🤰 FA is inherited in an autosomal recessive manner, which means that an individual develops FA only when he or she carries genetic defects in
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Molecular Characterizations of Fanconi Anemia Type A (FANCA) gene: Genetic heterogeneity of FANCA gene: Mohamed, Ream, Muddathir, Abdel Rahim, Fadl- Elmula, Imad: 9783639718331: Amazon.com: Books
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Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients | Haematologica
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Overwhelming genetic heterogeneity and exhausting molecular diagnostic process in chronic and progressive ataxias: facing it up with an algorithm, a gene, a panel at a time | Journal of Human Genetics
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PDF] Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics. | Semantic Scholar
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A defined role for multiple Fanconi anemia gene products in DNA-damage-associated ubiquitination - ScienceDirect
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