Screening for B cell, T cell and natural killer cell defects among children with methylmalonic and propionic acidemias
al-Abd, Hibah S., Rida, Shirin M., Hasan, Mahmud Abd, Salah al-Din, Ahmad M., al-Uwaidi, Rasha H.
Published in Egyptian Journal of Medical Human Genetics (06.09.2019)
Published in Egyptian Journal of Medical Human Genetics (06.09.2019)
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Journal Article
Serum amino acid abnormalities in pediatric patients with chronic renal failure with and without history of thromboembolic manifestations
El Sawy, Mohamad A., Zaki, Mona M., EL-Hakim, Ihab Z., Mowafy, Mohamad E., Al-Abd, Heba S.
Published in The Egyptian journal of medical human genetics (01.02.2012)
Published in The Egyptian journal of medical human genetics (01.02.2012)
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Journal Article
Familial Peters Plus syndrome with absent anal canal, sacral agenesis and sensorineural hearing loss: Expanding the clinical spectrum
Shawky, Rabah M., Elsayed, Solaf M., Abd-Elkhalek, Heba S., Gad, Shimaa
Published in The Egyptian journal of medical human genetics (01.10.2013)
Published in The Egyptian journal of medical human genetics (01.10.2013)
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Journal Article
Peters’ plus syndrome in an Egyptian patient with some unusual features
Shawqi, Rabah M., Abd al-Khaliq, Hibah S.
Published in The Egyptian journal of medical human genetics (01.05.2010)
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Published in The Egyptian journal of medical human genetics (01.05.2010)
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