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Egyptian Journal of Medical Human Genetics
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  1. Home /
  2. Archives /
  3. Vol. 11 No. 1 (2010)

Articles

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

Journal Identifiers


eISSN: 1110-8630

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