S. Ismail

Most-cited papers

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
E. Abdalla, A. Mostowska, P. Jagodziński, Karin Dwidar +1 more
2014Archives of Oral Biology29 citations
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Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights
M. S. Abdel-Hamid, S. Abdel-Ghafar, S. Ismail, Lubna M. Desouky +3 more
2020Clinical Genetics21 citations Open access
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Maternal serum alpha fetoprotein among pregnant females in Alexandria.
E. Baghagho, I. Kharboush, D. El-kaffash, T. Karkour +2 more
2004Journal of Egyptian Public Health Association10 citations
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Cytogenetic study in idiopathic infertile males.
S. Ismail, A. El-beheiry, M. M. Hashishe, M. E. el-Bahaei
1993Journal of Egyptian Public Health Association9 citations
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A diagnostic clinical genetic study of craniofacial dysmorphism.
H. Farag, S. Kotb, G. A. Sweify, R. Fawzy +1 more
1999Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit8 citations Open access
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Duplication 3q(q21----qter) without limb anomalies.
S. Ismail, B. Kousseff, S. Kotb, S. Kholeif
1991American journal of medical genetics8 citations
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Newborn screening for certain treatable inborn errors of metabolism in Alexandria.
S. Ismail, N. Abdelrahim, M. M. Hashishe, E. M. Abdallah
1996Journal of Egyptian Public Health Association4 citations
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Inheritance of non-syndromal genetic deafness.
S. Ismail, M. M. Hashine, M. Mourad, M. A. Kader
1996Journal of Egyptian Public Health Association4 citations
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Genetic diagnosis of Prader–Willi syndrome
A. Khedr, N. Meguid, A. Mohamed, S. Ismail +3 more
20163 citations
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Sister chromatid exchanges and chromosome aberrations in lymphocytes of medical personnel handling cytostatic drugs.
H. Mahrous, S. Ismail, M. M. Hashishe, H. M. Kohail
1998Journal of Egyptian Public Health Association3 citations
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Genetic Study of Syndromic Inherited Deafness
S. Ismail, M. M. Hashishe, M. Mourad, M. Abdelkader
20071 citations
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Chromosome damage in passive smoker females.
S. Ismail, S. Kholeif, M. Mokhtar
1998Journal of Egyptian Public Health Association1 citations
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Genetic Study of Multiple Congenital Contractures (Arthrogryposis Multiplex Congenita)
Mervat El Belbesy, S. Ismail, S. Kotb, Hassan El-Hosseiny +1 more
2003Journal of High Institute of Public Health0 citations
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Nucleolus organizer region heteromorphism in patients with Down syndrome and their parents.
N. Nazmy, S. Kotb, M. M. Mokhtar, S. Ismail
1999Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit0 citations
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GENETIC STUDY OF COUPLES WITH REPEATED SPONTANEOUS ABORTION IN ALEXANDRIA
M. M. Mokhtar, S. Kotb, Amal A. Abd El Aziz, S. Ismail
19960 citations
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Orodental and ultrastructural studies of pulp and gingiva in phenylketonuria.
E. Aboul-Ezz, E. Hilal, A. S. Girgis, S. Temtamy +2 more
1988Journal of Egyptian Public Health Association0 citations
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