Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.
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G. McLennan | A. R. Smith | D. Meyerholz | M. Welsh | G. Tearney | D. Stoltz | M. Suter | J. Zabner | P. McCray | S. Ramachandran | E. Namati | A. Pezzulo | S. Kao | M. Rector | Amanda R. Smith