Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population von Vallian Broojeni, Jalal, Kazemi, Arezu, Rezaei, Halimeh, Vallian, Sadeq

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Defects in meiosis I contribute to the genesis of androgenetic hydatidiform moles von Rezaei, Maryam, Liang, Manqi, Yalcin, Zeynep, Martin, Jacinta H, Kazemi, Parinaz, Bareke, Eric, Ge, Zhao-Jia, Fardaei, Majid, Benadiva, Claudio, Hemida, Reda, Hassan, Adnan, Maher, Geoffrey J, Abdalla, Ebtesam, Buckett, William, Bolze, Pierre-Adrien, Sandhu, Iqbaljit, Duman, Onur, Agrawal, Suraksha, Qian, JianHua, Vallian Broojeni, Jalal, Bhati, Lavi, Miron, Pierre, Allias, Fabienne, Selim, Amal, Fisher, Rosemary A, Seckl, Michael J, Sauthier, Philippe, Touitou, Isabelle, Tan, Seang Lin, Majewski, Jacek, Taketo, Teruko, Slim, Rima

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PLCZ1 Mutation and Failed IUI, ICSI, and Spontaneous Pregnancy Loss: Insights from a Case Study von Broojeni, Jalal Vallian, Safwat, Sylvia, Bareke, Eric, Majewski, Jacek, Abdalla, Ebtesam, Slim, Rima

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Defects in meiosis I contribute to the genesis of androgenetic hydatidiform moles von Rezaei, Maryam, Liang, Manqi, Yakin, Zeynep, Martin, Jacinta H, Kazemi, Parinaz, Bareke, Eric, Ge, Zhao-Jia, Fardaei, Majid, Benadiva, Claudio, Hemida, Reda, Hassan, Adnan, Maher, Geoffrey J, Abdalla, Ebtesam, Buckett, William, Bolze, Pierre-Adrien, Sandhu, Iqbaljit, Duman, Onur, Agrawal, Suraksha, Qian, Jianhua, Broojeni, Jalal Vallian, Bhati, Lavi, Miron, Pierre, Allias, Fabienne, Selim, Amal, Fisher, Rosemary A, Seckl, Michael J, Sauthier, Philippe, Touitou, Isabelle, Tan, Seang Lin, Majewski, Jacek, Taketo, Teruko, Slim, Rima

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