The Use of Fluorescence In situ Hybridisation in the Diagnosis of Hidden Mosaicism in Egyptian Patients with Turner Syndrome von Ossama, Heba Mohamed, Kholeif, Soha, Elhady, Ghada Mohamed

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Sperm chromosomal abnormalities in infertile men with failed intracytoplasmic sperm injection von Elnahas, Rania Fathy, Behery, Amal Kotb, Kholeif, Soha, Orief, Yasser Ibrahim, Elhady, Ghada Mohamed

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Chromosomal Aberrations in 224 Couples with Recurrent Pregnancy Loss von Elhady, Ghada Mohamed, Kholeif, Soha, Nazmy, Nahla

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CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma von Fassad, Mahmoud R., Amin, Asmaa K., Morsy, Heba A., Issa, Noha M., Bayoumi, Nader H., El Shafei, Sahar A., Kholeif, Soha F.

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Homozygosity for a Robertsonian Translocation (13q;14q) in an Otherwise Healthy 44, XY Man With a History of Repeated Fetal Losses von Abdalla, Ebtesam M, Kholeif, Soha F, Elshaffie, Reem M

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Detection of 35delG, 167delT mutations in the connexin 26 gene among Egyptian patients with nonsyndromic sensorineural hearing loss von El Barbary, Nehal E., El Belbesy, Mervat F., Asal, Samir I., Kholeif, Soha F.

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Familial reciprocal non robertsonian translocation t(14;22) resulting in 22q11.2 deletion syndrome von Nazmy, Nahla, Elhady, Ghada, Refaat, Esraa, Kholeif, Soha

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The Effect of Teratozoospermia on Sex Chromosomes in Human Embryos von Mostafa Nayel, Dalia, Salah El Din Mahrous, Hanan, El Din Khalifa, Emad, Kholeif, Soha, Mohamed Elhady, Ghada

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Duplication 3q(q21 → qter) without limb anomalies von Ismail, Suzan R., Kousseff, Boris G., Kotb, Samia M., Kholeif, Soha F.

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