Cite
HARVARD Citation
Kimble, D. et al. (2018). A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families. Human mutation. 39 (2), pp. 237-254. [Online].
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Kimble, D. et al. (2018). A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families. Human mutation. 39 (2), pp. 237-254. [Online].