IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short children
Fadel, Islam M., Ragab, Moustafa H., Eid, Ola M., Helmy, Nivine A., El-Bassyouni, Hala T., Mazen, Inas
Published in Journal of Genetic Engineering and Biotechnology (28.07.2021)
Published in Journal of Genetic Engineering and Biotechnology (28.07.2021)
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Journal Article
Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature
Mekkawy, Mona K., Kamel, Alaa K., Thomas, Manal M., Ashaat, Engy A., Zaki, Maha S., Eid, Ola M., Ismail, Samira, Hammad, Saida A., Megahed, Hisham, ElAwady, Heba, Refaat, Khaled M., Hussien, Shymaa, Helmy, Nivine, Abd Allah, Sally G., Mohamed, Amal M., El Ruby, Mona O.
Published in Molecular genetics & genomic medicine (01.02.2021)
Published in Molecular genetics & genomic medicine (01.02.2021)
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Journal Article
Hepatitis C virus and schistosomiasis as a causative factor for hTERT amplification in hepatocellular carcinoma
Eid, Ola M, Helmy, Nivine A, Fadel, Islam H, Ezzat, Waffa M, Kamel, Refaat R, Eid, Maha M
Published in Gene reports (01.12.2016)
Published in Gene reports (01.12.2016)
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Journal Article
Clinical and cytogenetic description of three patients with constitutional mosaic trisomy 8
Ismail, Samira, Kamel, Alaa K., Eid, Maha M., Elruby, Mona O., Aglan, Mona S., Mekkawy, Mona K., Zaki, Maha S., Mohamed, Amal M., Helmy, Nivine A., Temtamy, Samia A.
Published in Middle East Journal of Medical Genetics (01.01.2017)
Published in Middle East Journal of Medical Genetics (01.01.2017)
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Journal Article
Cytogenetics abnormalities in a referred population for chromosomal analysis and the role of fluorescence in-situ hybridization in refining the diagnosis
Mohamed, Amal M., Kamel, Alaa K., Helmy, Nivine A., Hammad, Saida, Kayed, Hesham F., Shihab, Marwa, El-Gerzawy, Assad, Eid, Maha M., Eid, Ola M., Mekkawy, Mona K., Mahmoud, Wael, Mazen, Inas, El-Ruby, Mona, Afifi, Hanan, Zaki, Maha, Salam, Ghada A., Aglan, Mona, Temtamy, Samia
Published in Middle East Journal of Medical Genetics (01.01.2017)
Published in Middle East Journal of Medical Genetics (01.01.2017)
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Journal Article
Phenotypic characterization of rare interstitial deletion of chromosome 4
Ismail, Samira, Helmy, Nivine A., Mahmoud, Wael M., El-Ruby, Mona O.
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.09.2012)
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.09.2012)
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Journal Article
Contribution of chromosomal abnormalities at 10q and 22q to autism
Meguid, Nagwa A., Eid, Maha M., Mohamed, Amal M., Ghanoum, Heba, Helmy, Nivine A., Eid, Ola M.
Published in Research in autism spectrum disorders (01.06.2018)
Published in Research in autism spectrum disorders (01.06.2018)
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Journal Article
Interstitial Deletion of 2q22.2q22.3 Involving the Entire ZEB2 Gene in a Case of Mowat-Wilson Syndrome
Refaat, Khaled, Helmy, Nivine, Elawady, Mohamed, El Ruby, Mona, Kamel, Alaa, Mekkawy, Mona, Ashaat, Engy, Eid, Ola, Mohamed, Amal, Rady, Mervat
Published in Molecular syndromology (01.04.2021)
Published in Molecular syndromology (01.04.2021)
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Journal Article
Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility
A. Abdel Kader, Rania, Eid, Maha, Eltoukhy, Safinaz, Helmy, Nivine, Abd El-Hamid, Mahmoud, Omar, Ahmed, Sherif, Naglaa, Mohamed, Magdy, Kayed, Hesham
Published in Middle East Journal of Medical Genetics (01.01.2021)
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Published in Middle East Journal of Medical Genetics (01.01.2021)
Journal Article
Cytogenetic study of a large cohort of patients with corpus callosum abnormalities
Hussen, Dalia, Kamel, Alaa, Mekkawy, Mona, Mohamed, Amal, Zaki, Maha, Issa, Mahmoud, El Ruby, Mona, Ashaat, Engy, Ismail, Samira, Refaat, Khaled, Helmy, Nivine
Published in Middle East Journal of Medical Genetics (01.07.2019)
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Published in Middle East Journal of Medical Genetics (01.07.2019)
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