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Showing below up to 50 results in range #6,701 to #6,750.

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  1. Other cyst of bone, carpus (Q106114)
  2. Skin manifestation of other specified neonatal mineral deficiency (Q106113)
  3. Haemoglobinuria from marching (Q106112)
  4. Ventral simultagnosia (Q106111)
  5. Ataxia oculomotor apraxia (Q106110)
  6. Other cyst of bone, radius (Q106109)
  7. Haemoglobinuria from exertion (Q106108)
  8. Other cyst of bone, clavicle (Q106107)
  9. Doubly committed juxta-arterial ventricular septal defect with posteriorly malaligned fibrous outlet septum (Q106106)
  10. Pale faeces (Q106105)
  11. Outlet muscular ventricular septal defect without malalignment (Q106104)
  12. Benign neoplasm of carina (Q106103)
  13. Doubly committed juxta-arterial ventricular septal defect without malalignment (Q106102)
  14. Outlet perimembranous ventricular septal defect with posteriorly malaligned outlet septum (Q106101)
  15. Benign neoplasm of main bronchus (Q106100)
  16. Solitary pulmonary hamartoma or chondroadenoma (Q106099)
  17. Outlet perimembranous ventricular septal defect with anteriorly malaligned outlet septum (Q106098)
  18. Benign neoplasm of hilus of lung (Q106097)
  19. Outlet muscular ventricular septal defect with posteriorly malaligned outlet septum (Q106096)
  20. Outlet muscular ventricular septal defect with anteriorly malaligned outlet septum (Q106095)
  21. Cyst of vocal cord (Q106094)
  22. Multiple pulmonary hamartomas or chondroadenomas (Q106093)
  23. Subepiglottic thickening (Q106092)
  24. Thickening of larynx (Q106091)
  25. Benign tumour of lung parenchyma (Q106090)
  26. Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum (Q106089)
  27. Chronic trochlear nerve palsy, spread of comitance (Q106088)
  28. Multiple pulmonary hyalinizing granuloma (Q106087)
  29. Single pulmonary hyalinizing granuloma (Q106086)
  30. Single pulmonary leiomyoma (Q106085)
  31. Post traumatic segmental ischemia or infarction of kidney (Q106084)
  32. Multiple pulmonary leiomyoma (Q106083)
  33. Xiphopagus (Q106082)
  34. Allan-Herndon-Dudley syndrome (Q106081)
  35. Post traumatic complete ischemia or infarction of kidney (Q106080)
  36. Pure mitochondrial myopathy (Q106079)
  37. Ureter infection (Q106078)
  38. Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (Q106077)
  39. Infectious diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis (Q106076)
  40. Young-Simpson syndrome (Q106075)
  41. Benign chorea - hypothyroidism (Q106074)
  42. Acrodysostosis with multiple hormone resistance (Q106073)
  43. Lethal infantile mitochondrial myopathy (Q106072)
  44. Generalised uridine diphosphate galactose-4-epimerase deficiency (Q106071)
  45. Kocher-Debre-Semelaigne syndrome (Q106070)
  46. Congenital hypothyroidism with chromosome abnormalities (Q106069)
  47. Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (Q106068)
  48. Noninfectious diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis (Q106067)
  49. Choreoathetosis - hypothyroidism - neonatal respiratory distress (Q106066)
  50. Reticular perineurioma (Q106065)

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