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Author/Creator Ben‐Yosef, Tamar

1. A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC). Issue 1 (15th September 2019)

Authors:
Sharon, Dror; Ben‐Yosef, Tamar; Goldenberg‐Cohen, Nitza; Pras, Eran; Gradstein, Libe; Soudry, Shiri; Mezer, Eedy; Zur, Dinah; Abbasi, Anan H.; Zeitz, Christina; Cremers, Frans P. M.; Khan, Muhammad I.; Levy, Jaime; Rotenstreich, Ygal; Birk, Ohad S.; Ehrenberg, Miriam; Leibu, Rina; Newman, Hadas; ...
Journal:
Human mutation
Issue:
Volume 41:Issue 1(2020)
Page Start:
140
Record Type:
Journal Article
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2. Homozygous deletion of TRMT10A as part of a contiguous gene deletion in a syndrome of failure to thrive, delayed puberty, intellectual disability and diabetes mellitus. (22nd August 2015)

Authors:
Zung, Amnon; Kori, Michal; Burundukov, Ella; Ben‐Yosef, Tamar; Tatoor, Yasmin; Granot, Esther
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 12(2015:Dec.)
Page Start:
3167
Record Type:
Journal Article
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