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8 results
  1. ... C11.270.660 Retinal Dysplasia C11.270.684 Retinitis Pigmentosa C11.270.684.249 Alstrom Syndrome C11.270. ... Cone-Rod Dystrophies C11.768.585.658.500 Retinitis Pigmentosa C11.768.585.658.500.627 Kearns-Sayre ...
  2. ... C11.270.660...........................................Retinal Dysplasia C11.270.684...........................................Retinitis Pigmentosa C11.270.684.249...........................................Alstrom Syndrome C11.270. ...
  3. ... Optic Atrophy, Hereditary, Leber Wolfram Syndrome Retinal Dysplasia Retinitis Pigmentosa Alstrom Syndrome Graves Ophthalmopathy Walker-Warburg Syndrome Weill- ...
  4. ... the MERTK gene are associated with type 38 RETINITIS PIGMENTOSA; it also plays a critical role as an ...
  5. ... and night blindness. AN: ROD CONE DYSTROPHIES see RETINITIS PIGMENTOSA is also available Tree locations: Eye Diseases, Hereditary ...
  6. ... in the infant and preschool child Auditory evoked RETINITIS pigmentosa RIGHTS of mentally handicapped patients ROLE of interferon ...
  7. ... in the infant and preschool child Auditory evoked RETINITIS pigmentosa RIGHT TO DIE Euthanasia and the RIGHTS of ...
  8. ... rehabilitation, services (with emphasis on the U.S.) Mental RETINITIS pigmentosa RIGHTS of mentally hand!canoed patients SAFETY, regulation ...