All Stories

  1. Compound heterozygous mutations in theIFT140gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy

    Article • Clinical Genetics, February 2017, Wiley

    Dr Christian Peña-Padilla

  2. Descriptive study of the complete blood count in newborn infants with Down syndrome

    Article • American Journal of Medical Genetics Part A, February 2017, Wiley

    Dra Mireya Orozco, Dr Christian Peña-Padilla