Soe, K., & Gregoire‐Bottex, M. M. (2017). A rare CFTR mutation associated with severe disease progression in a 10‐year‐old Hispanic patient. Clin Case Rep.
Chicago Style aipamenaSoe, Katherine, and M. Myrtha Gregoire‐Bottex. "A Rare CFTR Mutation Associated With Severe Disease Progression in a 10‐year‐old Hispanic Patient." Clin Case Rep 2017.
MLA aipamenaSoe, Katherine, and M. Myrtha Gregoire‐Bottex. "A Rare CFTR Mutation Associated With Severe Disease Progression in a 10‐year‐old Hispanic Patient." Clin Case Rep 2017.
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