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The phenotype of 15 cases with rare 8q24.13-q24.3 deletions–A new syndrome or still an enigma?
Idit Maya, Sarit Kahana, Ifaat Agmon-Fishman, Cochava Klein, Reut Matar, Racheli Berger, Sagi Ben Yehoshua Josefsberg, Mordechai Shohat, Daphna Marom, Lina Basel-Salmon, Lena Sagi-Dain*
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review