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Author/Creator Beryozkin, Avigail

1. 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. Nonsyndromic Early‐Onset Cone‐Rod Dystrophy and Limb‐Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF. Issue 9 (14th July 2015)

Authors:
Lazar, Csilla H.; Kimchi, Adva; Namburi, Prasanthi; Mutsuddi, Mousumi; Zelinger, Lina; Beryozkin, Avigail; Ben‐Simhon, Shiran; Obolensky, Alexey; Ben‐Neriah, Ziva; Argov, Zohar; Pikarsky, Eli; Fellig, Yakov; Marks‐Ohana, Devorah; Ratnapriya, Rinki; Banin, Eyal; Sharon, Dror; Swaroop, Anand
Journal:
Human mutation
Issue:
Volume 36:Issue 9(2015:Sep.)
Page Start:
836
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗