Karen J. Heath-rekin lankidetzan egindako argitalpenak (2)

2018

  1. Erratum: Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features (The American Journal of Human Genetics (2018) 103(5) (786–793), (S0002929718303239), (10.1016/j.ajhg.2018.09.012))

    American Journal of Human Genetics

  2. 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, Núm. 5, pp. 786-793