Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

著者: Amir, R, Fang, P, Yu, Z, Glaze, D, Percy, A, Zoghbi, H, Roa, B, Van den Veyver, I B
出版事項 2005

No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility

著者: Aghajanova, L., Mahadevan, S., Altmäe, S., Stavreus-Evers, A., Regan, L., Sebire, N., Dixon, P., Fisher, R.A., Van den Veyver, I.B.
出版年 Hum Reprod (2015)