Eid MM - Search Results

1

Detection of AZFc gene deletion in a cohort of Egyptian patients with idiopathic male infertility.

Eid MM, Eid OM, Abdelrahman AH, Abdelrahman IFS, Aboelkomsan EAF, AbdelKader RMA, Hassan M, Farid M, Ibrahim AA, Abd El-Fattah SN, Mahrous R. Eid MM, et al. Among authors: eid om. J Genet Eng Biotechnol. 2023 Nov 10;21(1):111. doi: 10.1186/s43141-023-00584-9. J Genet Eng Biotechnol. 2023. PMID: 37947911 Free PMC article.

2

A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder.

Abdel-Salam GM, Miyake N, Eid MM, Abdel-Hamid MS, Hassan NA, Eid OM, Effat LK, El-Badry TH, El-Kamah GY, El-Darouti M, Matsumoto N. Abdel-Salam GM, et al. Among authors: eid om, eid mm. Am J Med Genet A. 2011 Nov;155A(11):2885-96. doi: 10.1002/ajmg.a.34299. Epub 2011 Oct 11. Am J Med Genet A. 2011. PMID: 21990275

3

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

4

Detection of cytogenetics abnormalities in chronic lymphocytic leukemia using FISH technique and their prognostic impact.

Eid OM, Eid MM, Kayed HF, Mahmoud WM, Mousafa SS, Ismail MM, Abdeen DM. Eid OM, et al. Among authors: eid mm. Gulf J Oncolog. 2014 Jan;1(15):68-75. Gulf J Oncolog. 2014. PMID: 24610291

5

De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features.

Afifi HH, Fukai R, Miyake N, Gamal El Din AA, Eid MM, Eid OM, Thomas MM, El-Badry TH, Tosson AM, Abdel-Salam GM, Matsumoto N. Afifi HH, et al. Among authors: eid om, eid mm. Am J Med Genet A. 2015 Oct;167A(10):2418-24. doi: 10.1002/ajmg.a.37185. Epub 2015 May 31. Am J Med Genet A. 2015. PMID: 26033841

6

Evaluation of BRCA1 Large Genomic Rearrangements in Group of Egyptian Female Breast Cancer Patients Using MLPA.

Eid OM, El Ghoroury EA, Eid MM, Mahrous RM, Abdelhamid MI, Aboafya ZI, Abdel Ghaffar EA, Abdelrahman AH. Eid OM, et al. Among authors: eid mm. Gulf J Oncolog. 2017 Sep;1(25):64-69. Gulf J Oncolog. 2017. PMID: 29019333

7

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. Neuropediatrics. 2020 Feb;51(1):76-82. doi: 10.1055/s-0039-1698421. Epub 2019 Oct 21. Neuropediatrics. 2020. PMID: 31634935

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. Among authors: eid om, eid mm. 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

Altered Expression of MicroRNAs in the Bone Marrow of Multiple Myeloma Patients and their Relationship to Cytogenetic Aberrations.

Attia HRM, Abdelrahman AH, Ibrahim MH, Eid MM, Eid OM, Sallam MT, El Gammal MM, Kamel MM. Attia HRM, et al. Among authors: eid om, eid mm. Curr Pharm Biotechnol. 2020;21(13):1394-1401. doi: 10.2174/1389201021666200320135139. Curr Pharm Biotechnol. 2020. PMID: 32196445

10

Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.

Eid MM, Eid OM, Abdel-Hadi S, Hassib N, Madian A, Afifi HH, Abdel-Salam GMH. Eid MM, et al. Among authors: eid om. J Pediatr Genet. 2020 Sep;9(3):207-210. doi: 10.1055/s-0039-3400489. Epub 2019 Nov 21. J Pediatr Genet. 2020. PMID: 32714624 Free PMC article.

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