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Ito, Yoko, Carss, Keren J, Duarte, Sofia T, Hartley, Taila, Keren, Boris, Kurian, Manju A, Marey, Isabelle, Charles, Perinne, Mendonça, Carla ORCID: 0000-0001-9926-0598, Nava, Caroline
et al (show 11 more authors) (2018) De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. American journal of human genetics, 103 (1). 144 - 153.


Kirschner, Kristina, Samarajiwa, Shamith A, Cairns, Jonathan M, Menon, Suraj, Perez-Mancera, Pedro A, Tomimatsu, Kosuke, Bermejo-Rodriguez, Camino, Ito, Yoko, Chandra, Tamir, Narita, Masako
et al (show 6 more authors) (2015) Phenotype Specific Analyses Reveal Distinct Regulatory Mechanism for Chronically Activated p53. PLOS GENETICS, 11 (3).

This list was generated on Wed Nov 11 06:19:28 2020 GMT.