Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features - Peter D. Turnpenny, Michael J. Wright, Melissa Sloman, Anthony J. van Essen, Erica Gerkes, Rolph Pfundt, Susan M. White, Nava Shaul-Lotan, G. Bradley Schaefer, Alan Fryer, A. Micheil Innes, Heather McLaughlin, Lindsay B. Henderson, Amy E. Roberts, Karen E. Heath - Dissemin

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Cell Press, American Journal of Human Genetics, 6(103), p. 1054-1055, 2018

DOI: 10.1016/j.ajhg.2018.11.009

Cell Press, American Journal of Human Genetics, 5(103), p. 786-793, 2018

DOI: 10.1016/j.ajhg.2018.09.012

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Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features

Journal article published in 2018 by Peter D. Turnpenny, Michael J. Wright, Melissa Sloman, Anthony J. van Essen, Erica Gerkes, Rolph Pfundt, Susan M. White, Nava Shaul-Lotan, G. Bradley Schaefer, Alan Fryer, A. Micheil Innes, Heather McLaughlin, Lindsay B. Henderson, Amy E. Roberts, Karen E. Heath and other authors.

This paper was not found in any repository, but could be made available legally by the author.

This paper was not found in any repository, but could be made available legally by the author.

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