Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statementFrédéric Brioude, Eamonn R. Maher, Jennifer M. Kalish et al.|Nature Reviews Endocrinology|2018Cited by 596
Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and MacrocephalyMaila Giannandrea, Patrizia D’Adamo, Francesca Cogliati et al.|The American Journal of Human Genetics|2010Cited by 238
Recommendations of the Scientific Committee of the Italian Beckwith–Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndromeAlessandro Mussa, Giovanni Battista Ferrero, Stefania Di Candia et al.|European Journal of Medical Genetics|2015Cited by 92
Taurine Administration Recovers Motor and Learning Deficits in an Angelman Syndrome Mouse ModelSara Guzzetti, Silvia Russo|International Journal of Molecular Sciences|2018Cited by 19