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A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies
Pode-Shakked, Ben, Barel, Ortal, Singer, Amihood, Regev, Miriam, Poran, Hana, Eliyahu, Aviva, Finezilber, Yael, Segev, Meirav, Berkenstadt, Michal, Yonath, Hagith, Reznik-Wolf, Haike, Gazit, Yael, Chorin, Odelia, Heimer, Gali, Gabis, Lidia V., Tzadok, Michal, Nissenkorn, Andreea, Bar-Yosef, Omer, Zohar-Dayan, Efrat, Ben-Zeev, Bruria, Mor, Nofar, Kol, Nitzan, Nayshool, Omri, Shimshoviz, Noam, Bar-Joseph, Ifat, Marek-Yagel, Dina, Javasky, Elisheva, Einy, Reviva, Gal, Moran, Grinshpun-Cohen, Julia, Shohat, Mordechai, Dominissini, Dan, Raas-Rothschild, Annick, Rechavi, Gideon, Pras, Elon, Greenbaum, Lior
Published in Scientific reports (27.09.2021)
Published in Scientific reports (27.09.2021)
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Journal Article
Identification of recurrent pathogenic alleles using exome sequencing data: Proof-of-concept study of Russian subjects
Orlov, Igor E., Laidus, Tatiana A., Tumakova, Anastasia V., Yanus, Grigoriy A., Iyevleva, Aglaya G., Sokolenko, Anna P., Bizin, Ilya V., Imyanitov, Evgeny N., Suspitsin, Evgeny N.
Published in European journal of medical genetics (01.02.2022)
Published in European journal of medical genetics (01.02.2022)
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Journal Article