Articles

• Severe congenital neutropenia (Kostmann Syndrome)

  SK Al-Jaouni

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• Genomics in health and disease

  RM Shawky, SMN El Din

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• L–Carnitine ameliorates the iron mediated DNA degradation in peripheral leukocytes of β-thalassemic children

  SM Ragab, RG Mahfouz

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• Gene polymorphisms of TNF-α and IL-10 related to rheumatic heart disease

  E Tawfik, MA El–Salam, A Abdulkarem, M Yosseri

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• Genetic study of congenital limb anomalies among Egyptian children

  RM Shawky, HMF Karara, MSZ Salem

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• Common MEFV mutations in Egyptian patients with familial Mediterranean fever

  M El Sayed, N Elazizi, AM Ibrahim, T Zaher, M Hashem

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• Peters’ plus syndrome in an Egyptian patient with some unusual features

  R Shawky, HS Abd-Elkhalek

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• Progressive osseous heteroplasia (POH): an Egyptian patient

  E El Sobky, SM El Sayed

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• Corpus callosum defect with dilated lateral ventricles and an occipital cyst in an Egyptian child with Diamond-Blackfan anemia

  R Shawky, N El-Sayed

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