Information Journal Paper
APA:
Copy. (2018). A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families. Human Mutation, 39(2), 237-254. SID. https://sid.ir/paper/757011/en
Vancouver:
Copy. A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families. Human Mutation[Internet]. 2018;39(2):237-254. Available from: https://sid.ir/paper/757011/en
IEEE:
Copy, “A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families,” Human Mutation, vol. 39, no. 2, pp. 237–254, 2018, [Online]. Available: https://sid.ir/paper/757011/en