A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes
采用多种方法对 Silver-Russell 综合征和 Beckwith-Wiedemann 综合征所致的明显和边缘性 11p15.5 缺陷进行分子诊断
期刊:Clinical Epigenetics
影响因子:
doi:10.1186/s13148-016-0183-8
Silvia Russo #, Luciano Calzari #, Alessandro Mussa, Ester Mainini, Matteo Cassina, Stefania Di Candia, Maurizio Clementi, Sara Guzzetti, Silvia Tabano, Monica Miozzo, Silvia Sirchia, Palma Finelli, Paolo Prontera, Silvia Maitz, Giovanni Sorge, Annalisa Calcagno, Mohamad Maghnie, Maria Teresa Divizi
