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Author/Creator Sayed, Inas S. M.

1. Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9‐associated disease trait. Issue 2 (10th November 2021)

Authors:
Abdel‐Salam, Ghada M. H.; Duan, Ruizhi; Abdel‐Hamid, Mohamed S.; Sayed, Inas S. M.; Jhangiani, Shalini N.; Khan, Ziad; Du, Haowei; Gibbs, Richard A.; Posey, Jennifer E.; Marafi, Dana; Lupski, James R.
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 2(2022)
Page Start:
648
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation. Issue 6 (8th April 2020)

Authors:
Abdel‐Salam, Ghada M. H.; Sayed, Inas S. M.; Afifi, Hanan H.; Abdel‐Ghafar, Sherif F.; Abouzaid, Maha R.; Ismail, Samira I.; Aglan, Mona S.; Issa, Mahmoud Y.; EL‐Bassyouni, Hala T.; El‐Kamah, Ghada; Effat, Laila K.; Eid, Maha; Zaki, Maha S.; Temtamy, Samia A.; Abdel‐Hamid, Mohamed S.
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 6(2020)
Page Start:
1407
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Phenotypic and molecular insights into PQBP1‐related intellectual disability. Issue 11 (23rd September 2018)

Authors:
Abdel‐Salam, Ghada M. H.; Miyake, Noriko; Abdel‐Hamid, Mohamed S.; Sayed, Inas S. M.; Gadelhak, Mohamed I.; Ismail, Samira I.; Aglan, Mona S.; Afifi, Hanan H.; Temtamy, Samia A.; Matsumoto, Naomichi
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 11(2018)
Page Start:
2446
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗