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Author/Creator Hadar, Noam

1. B4GALT1‐congenital disorders of glycosylation: Expansion of the phenotypic and molecular spectrum and review of the literature. Issue 6 (16th March 2020)

Authors:
Staretz‐Chacham, Orna; Noyman, Iris; Wormser, Ohad; Abu Quider, Abed; Hazan, Guy; Morag, Iris; Hadar, Noam; Raymond, Kimiyo; Birk, Ohad S.; Ferreira, Carlos R.; Koifman, Arie
Journal:
Clinical genetics
Issue:
Volume 97:Issue 6(2020)
Page Start:
920
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. PSMC1 variant causes a novel neurological syndrome. Issue 4 (3rd August 2022)

Authors:
Aharoni, Sarit; Proskorovski‐Ohayon, Regina; Krishnan, Ramesh Kumar; Yogev, Yuval; Wormser, Ohad; Hadar, Noam; Bakhrat, Anna; Alshafee, Ismael; Gombosh, Maya; Agam, Nadav; Gradstein, Libe; Shorer, Zamir; Zarivach, Raz; Eskin‐Schwartz, Marina; Abdu, Uri; Birk, Ohad S.
Journal:
Clinical genetics
Issue:
Volume 102:Issue 4(2022)
Page Start:
324
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗