Cite
Turnpenny PD, Wright MJ, Sloman M, et al. Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features. Am J Hum Genet. 2018;103(5):786-793doi: 10.1016/j.ajhg.2018.09.012.
Turnpenny, P. D., Wright, M. J., Sloman, M., Caswell, R., van Essen, A. J., Gerkes, E., Pfundt, R., White, S. M., Shaul-Lotan, N., Carpenter, L., Schaefer, G. B., Fryer, A., Innes, A. M., Forbes, K. P., Chung, W. K., McLaughlin, H., Henderson, L. B., Roberts, A. E., Heath, K. E., Paumard-Hernández, B., Gener, B., Fawcett, K. A., Gjergja-Juraški, R., Pilz, D. T., & Fry, A. E. (2018). Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features. American journal of human genetics, 103(5), 786-793. https://doi.org/10.1016/j.ajhg.2018.09.012
Turnpenny, Peter D, et al. "Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features." American journal of human genetics vol. 103,5 (2018): 786-793. doi: https://doi.org/10.1016/j.ajhg.2018.09.012
Turnpenny PD, Wright MJ, Sloman M, Caswell R, van Essen AJ, Gerkes E, Pfundt R, White SM, Shaul-Lotan N, Carpenter L, Schaefer GB, Fryer A, Innes AM, Forbes KP, Chung WK, McLaughlin H, Henderson LB, Roberts AE, Heath KE, Paumard-Hernández B, Gener B, Fawcett KA, Gjergja-Juraški R, Pilz DT, Fry AE. Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features. Am J Hum Genet. 2018 Nov 01;103(5):786-793. doi: 10.1016/j.ajhg.2018.09.012. Epub 2018 Oct 18. PMID: 30343942; PMCID: PMC6218713.
Copy
Download .nbib