Eid O - Search Results

1

Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation.

Mohamed AM, El-Bassyouni HT, El-Gerzawy AM, Hammad SA, Helmy NA, Kamel AK, Ismail SI, Issa MY, Eid O, Zaki MS. Mohamed AM, et al. Among authors: eid o. Mol Cytogenet. 2018 Nov 6;11:57. doi: 10.1186/s13039-018-0406-0. eCollection 2018. Mol Cytogenet. 2018. PMID: 30410579 Free PMC article.

2

Cyclin D1 gene amplification in proliferating haemangioma.

Mohamed AM, Elwakil TF, Taher IM, Elbarbary MM, Kayed HF, Hussein HA, Eid OM. Mohamed AM, et al. Cell Tissue Res. 2009 Oct;338(1):107-15. doi: 10.1007/s00441-009-0858-y. Epub 2009 Sep 9. Cell Tissue Res. 2009. PMID: 19823825

3

Clinical and cytogenetic study of a non mosaic 46, X, isodicentric Yq in an Egyptian patient with Turner syndrome.

El-Bassyouni HT, El-Gerzawy A, Eid O, El-Ruby MO. El-Bassyouni HT, et al. Among authors: eid o. Genet Couns. 2013;24(1):37-44. Genet Couns. 2013. PMID: 23610863

4

Ring chromosome 15: expanding the phenotype.

Eid MM, El-Bassyouni HT, Eid OM, Hamad SA, Elgerzawy A, Zaki MS, El-Ruby M. Eid MM, et al. Among authors: eid om. Genet Couns. 2013;24(4):417-25. Genet Couns. 2013. PMID: 24551985

5

Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt.

Eid OM, Abdel Hady S, El-Kotoury A, Said KA, Rafat K, El-Bassyouni HT. Eid OM, et al. Ophthalmic Genet. 2017 Sep-Oct;38(5):418-421. doi: 10.1080/13816810.2016.1247460. Epub 2017 Jan 20. Ophthalmic Genet. 2017. PMID: 28107085

6

Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion.

Eid M, Eid O, Hegazy I, Girgis M, Mohamed A, Abdel-Salam GMH. Eid M, et al. Among authors: eid o. Neuropediatrics. 2020 Feb;51(1):76-82. doi: 10.1055/s-0039-1698421. Epub 2019 Oct 21. Neuropediatrics. 2020. PMID: 31634935

7

Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features.

Zaki MS, Eid OM, Eid MM, Mohamed AM, Sayed ISM, Abdel-Hamid MS, Abdel-Salam GMH. Zaki MS, et al. Cytogenet Genome Res. 2019;159(3):130-136. doi: 10.1159/000504075. Epub 2019 Nov 13. Cytogenet Genome Res. 2019. PMID: 31715598

8

Detection of low-grade mosaicism and its correlation with hormonal profile, testicular volume, and semen quality in a cohort of Egyptian Klinefelter and Klinefelter-like patients.

Madian A, Eid MM, Shahin AAB, Mazen I, El-Bassyouni HT, Eid OM. Madian A, et al. Reprod Biol. 2020 Jun;20(2):259-263. doi: 10.1016/j.repbio.2020.02.002. Epub 2020 Feb 27. Reprod Biol. 2020. PMID: 32115387

9

Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.

Mekkawy MK, Kamel AK, Thomas MM, Ashaat EA, Zaki MS, Eid OM, Ismail S, Hammad SA, Megahed H, ElAwady H, Refaat KM, Hussien S, Helmy N, Abd Allah SG, Mohamed AM, El Ruby MO. Mekkawy MK, et al. Among authors: eid om. Mol Genet Genomic Med. 2021 Feb;9(2):e1546. doi: 10.1002/mgg3.1546. Epub 2020 Nov 20. Mol Genet Genomic Med. 2021. PMID: 33217222 Free PMC article. Review.

10

Interstitial Deletion of 2q22.2q22.3 Involving the Entire ZEB2 Gene in a Case of Mowat-Wilson Syndrome.

Refaat K, Helmy N, Elawady M, El Ruby M, Kamel A, Mekkawy M, Ashaat E, Eid O, Mohamed A, Rady M. Refaat K, et al. Among authors: eid o. Mol Syndromol. 2021 Apr;12(2):87-95. doi: 10.1159/000513313. Epub 2021 Mar 1. Mol Syndromol. 2021. PMID: 34012377 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

37 results

Search Page

Filters