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Date 2016 Author/Creator Sharon, Dror

2. Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data. Issue 9 (22nd April 2016)

Authors:
Khateb, Samer; Hanany, Mor; Khalaileh, Ayat; Beryozkin, Avigail; Meyer, Segev; Abu-Diab, Alaa; Abu Turky, Fathieh; Mizrahi-Meissonnier, Liliana; Lieberman, Sari; Ben-Yosef, Tamar; Banin, Eyal; Sharon, Dror
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 9(2016)
Page Start:
600
Record Type:
Journal Article
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3. Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. Issue 1 (December 2016)

Authors:
Gradstein, Libe; Zolotushko, Jenny; Sergeev, Yuri; Lavy, Itay; Narkis, Ginat; Perez, Yonatan; Guigui, Sarah; Sharon, Dror; Banin, Eyal; Walter, Eyal; Lifshitz, Tova; Birk, Ohad
Journal:
BMC medical genetics
Issue:
Volume 17:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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