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Online Medical Forum > Library Database Of Journals Publications Researches Category > Library Database Of Journals Publications Researches > Medicine Category > Internal Medicine Forum > Medicine Topics > Apert-Syndrome
  1. Apert-Syndrome: Apert syndrome with cerebellar changes (0 replies)
  2. Apert-Syndrome: Successful isotretinoin treatment of acne in a patient with apert syndrome. (0 replies)
  3. Apert-Syndrome: Evidence that fgf10 contributes to the skeletal and visceral defects of an apert syndrome mouse model (0 replies)
  4. Apert-Syndrome: Syndromes, disorders and maternal risk factors associated with neural tube defects (vii). (0 replies)
  5. Apert-Syndrome: Rare mutations of fgfr2 causing apert syndrome: identification of the first partial gene deletion, and an alu element insertion from a new subfamily (0 replies)
  6. Apert-Syndrome: Axillary osmidrosis in apert syndrome: management with an arthroscopic shaver technique. (0 replies)
  7. Apert-Syndrome: 'my aim is to get a boyfriend' (0 replies)
  8. Apert-Syndrome: [malformations of the lower extremities.] (0 replies)
  9. Apert-Syndrome: A population-based study of craniosynostosis in metropolitan atlanta, 1989-2003 (0 replies)
  10. Apert-Syndrome: Monozygotic twins with apert syndrome. (0 replies)
  11. Apert-Syndrome: Tracheal anomalies complicating ventilation of an infant with apert syndrome. (0 replies)
  12. Apert-Syndrome: Apert syndrome (0 replies)
  13. Apert-Syndrome: Apert syndrome (0 replies)
  14. Apert-Syndrome: A pro253arg mutation in fibroblast growth factor receptor 2 (fgfr2) causes skeleton malformation mimicking human apert syndrome by affecting both chondrogenesis and osteogenesis. (0 replies)
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