XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription

Por Zangen, David, Kaufman, Yotam, Zeligson, Sharon, Perlberg, Shira, Fridman, Hila, Kanaan, Moein, Abdulhadi-Atwan, Maha, Abu Libdeh, Abdulsalam, Gussow, Ayal, Kisslov, Irit, Carmel, Liran, Renbaum, Paul, Levy-Lahad, Ephrat
Publicado em 2011

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection

Por Aran, Adi, Rosenfeld, Nuphar, Jaron, Ranit, Renbaum, Paul, Zuckerman, Shachar, Fridman, Hila, Zeligson, Sharon, Segel, Reeval, Kohn, Yoav, Kamal, Lara, Kanaan, Moien, Segev, Yoram, Mazaki, Eyal, Rabinowitz, Ron, Shen, Ori, Lee, Ming, Walsh, Tom, King, Mary Claire, Gulsuner, Suleyman, Levy-Lahad, Ephrat
Publicado no Neurology (2016)