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Table of Contents
Articles
| Severe congenital neutropenia (Kostmann Syndrome) |
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| SK Al-Jaouni |
| Genomics in health and disease |
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| RM Shawky, SMN El Din |
| L–Carnitine ameliorates the iron mediated DNA degradation in peripheral leukocytes of β-thalassemic children |
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| SM Ragab, RG Mahfouz |
| Gene polymorphisms of TNF-α and IL-10 related to rheumatic heart disease |
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| E Tawfik, MA El–Salam, A Abdulkarem, M Yosseri |
| Genetic study of congenital limb anomalies among Egyptian children |
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| RM Shawky, HMF Karara, MSZ Salem |
| Common MEFV mutations in Egyptian patients with familial Mediterranean fever |
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| M El Sayed, N Elazizi, AM Ibrahim, T Zaher, M Hashem |
| Peters’ plus syndrome in an Egyptian patient with some unusual features |
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| R Shawky, HS Abd-Elkhalek |
| Progressive osseous heteroplasia (POH): an Egyptian patient |
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| E El Sobky, SM El Sayed |
| Corpus callosum defect with dilated lateral ventricles and an occipital cyst in an Egyptian child with Diamond-Blackfan anemia |
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| R Shawky, N El-Sayed |
ISSN: 1110-8630
