Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights
Abdel‐Hamid, Mohamed S., Abdel‐Ghafar, Sherif F., Ismail, Suzan R., Desouky, Lubna M., Issa, Mahmoud Y., Effat, Laila K., Zaki, Maha S.
Published in Clinical genetics (01.11.2020)
Published in Clinical genetics (01.11.2020)
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A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family
Abdalla, Ebtesam M, Mostowska, Adrianna, Jagodziński, Paweł P, Dwidar, Karin, Ismail, Suzan R
Published in Archives of oral biology (01.07.2014)
Published in Archives of oral biology (01.07.2014)
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Genetic diagnosis of Prader–Willi syndrome
Khedr, Azzah A., Meguid, Nagwa A., Mohamed, Amal M., Ismail, Suzan R., Nazmy, Nahla A., Hassan, Heba A., Essawi, Mona L.
Published in Middle East Journal of Medical Genetics (01.07.2016)
Published in Middle East Journal of Medical Genetics (01.07.2016)
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Duplication 3q(q21----qter) without limb anomalies
Ismail, S R, Kousseff, B G, Kotb, S M, Kholeif, S F
Published in American journal of medical genetics (15.03.1991)
Published in American journal of medical genetics (15.03.1991)
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