A multiplexed screening method for pluripotency

by Alexander Plotnikov, Noga Kozer, Vladislav Krupalnik, Shani Peles, Nofar Mor, Yoach Rais, Jacob H. Hanna, Haim M. Barr
Published 2017-08-01

GATA2 Deficiency in Adult Life Is Characterized by Phenotypic Diversity and Delayed Diagnosis

by Oded Shamriz, Oded Shamriz, Naseem Zahalka, Amos J. Simon, Amos J. Simon, Atar Lev, Atar Lev, Ortal Barel, Ortal Barel, Nofar Mor, Nofar Mor, Yuval Tal, Michael J. Segel, Michael J. Segel, Raz Somech, Raz Somech, Hagith Yonath, Hagith Yonath, Hagith Yonath, Ori Toker
Published 2022-05-01

A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies

by Ben Pode-Shakked, Ortal Barel, Amihood Singer, Miriam Regev, Hana Poran, Aviva Eliyahu, Yael Finezilber, Meirav Segev, Michal Berkenstadt, Hagith Yonath, Haike Reznik-Wolf, Yael Gazit, Odelia Chorin, Gali Heimer, Lidia V. Gabis, Michal Tzadok, Andreea Nissenkorn, Omer Bar-Yosef, Efrat Zohar-Dayan, Bruria Ben-Zeev, Nofar Mor, Nitzan Kol, Omri Nayshool, Noam Shimshoviz, Ifat Bar-Joseph, Dina Marek-Yagel, Elisheva Javasky, Reviva Einy, Moran Gal, Julia Grinshpun-Cohen, Mordechai Shohat, Dan Dominissini, Annick Raas-Rothschild, Gideon Rechavi, Elon Pras, Lior Greenbaum
Published 2021-09-01