Items without sitelinks

From determinar.ia.br - Determine suas informações

Showing below up to 50 results in range #10,901 to #10,950.

View ( | ) (20 | 50 | 100 | 250 | 500)

  1. Congenital atresia of pulmonary vein (Q101909)
  2. Mucopolysaccharidoses with prominent cutaneous features (Q101908)
  3. Oesophageal squamous cell carcinoma in situ (Q101907)
  4. Acral persistent papular mucinosis (Q101906)
  5. Self-healing juvenile cutaneous mucinosis (Q101905)
  6. Lipogranuloma (Q101904)
  7. Invasive aspergillosis of the upper respiratory tract (Q101903)
  8. Squamous intraepithelial neoplasia of oesophagus, high grade (Q101902)
  9. Idiopathic follicular mucinosis (Q101901)
  10. Secondary catabolic cutaneous mucinosis (Q101900)
  11. Focal primary metabolic cutaneous mucinosis (Q101899)
  12. Invasive Aspergillus tracheobronchitis (Q101898)
  13. Invasive aspergillosis of the larynx (Q101897)
  14. Paraffinoma (Q101896)
  15. Invasive aspergillosis of paranasal sinuses (Q101895)
  16. Folinic acid-responsive seizures (Q101894)
  17. Aspergillus mastoiditis (Q101893)
  18. Congenital anomaly of inferior caval vein (Q101892)
  19. Mycotic corneal ulcer due to Aspergillus species (Q101891)
  20. Aspergillus keratitis (Q101890)
  21. Persistent fever (Q101889)
  22. African iron overload (Q101888)
  23. Dietary haemosiderosis (Q101887)
  24. Congenital anomaly of the coronary sinus (Q101886)
  25. Aspergillus endophthalmitis (Q101885)
  26. Invasive renal aspergillosis (Q101884)
  27. Aspergillus epidural abscess (Q101883)
  28. Fever with rigors (Q101882)
  29. Aspergillus osteomyelitis (Q101881)
  30. Aspergillus thyroid abscess (Q101880)
  31. Congenital anomaly of superior caval vein (Q101879)
  32. Fever with chills (Q101878)
  33. Aspergillus endocarditis (Q101877)
  34. Rupture of marginal sinus affecting fetus or newborn (Q101876)
  35. Ehlers-Danlos syndrome with periventricular heterotopia (Q101875)
  36. Mitochondrial Membrane Protein-Associated Neurodegeneration (Q101874)
  37. Abruptio placentae affecting fetus or newborn (Q101873)
  38. Ehlers-Danlos syndrome, spondylocheirodysplastic type (Q101872)
  39. Beta-Propeller protein-associated neurodegeneration (Q101871)
  40. COASY Protein-Associated Neurodegeneration (Q101870)
  41. Ehlers-Danlos syndrome, arthrochalasic type (Q101869)
  42. Ehlers-Danlos syndrome, kyphoscoliotic type (Q101868)
  43. Ehlers-Danlos syndrome due to tenascin-X deficiency (Q101867)
  44. Ehlers-Danlos syndrome, cardiac valvular type (Q101866)
  45. Ehlers-Danlos syndrome, classic-like type (Q101865)
  46. Agnogenic myeloid metaplasia (Q101864)
  47. Myelogenous metaplasia (Q101863)
  48. Pantothenate-kinase-associated neurodegeneration (Q101862)
  49. Ehlers-Danlos syndrome, dysfibronectinaemic type (Q101861)
  50. Ablatio placentae affecting fetus or newborn (Q101860)

View ( | ) (20 | 50 | 100 | 250 | 500)