Results 1 - 10 of 11 for 1E -"4-hydroxy-1-(4-methoxyphenyl)pent-1-en-3-one"
  1. ... type IE Hereditary sensory and autonomic neuropathy type 1E Disease InfoSearch National Organization for Rare Disorders (NORD) ... spot mutation in hereditary sensory and autonomic neuropathy 1E. Epigenetics. 2014 Aug;9(8):1184-93. doi: ...
  2. ... Genetic Testing Registry: Congenital stationary night blindness, type 1E Genetic Testing Registry: Congenital stationary night blindness, type ... STATIONARY, TYPE 1D NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F PubMed Audo ...
  3. Usher Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Usher Syndrome/Learn More ... Usher Syndrome ... A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information ...
  4. ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Sjöholm AG, Jönsson G, Braconier ...
  5. ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Krishnan V, Xu Y, Macon ...
  6. ... CARDIOMYOPATHY, DILATED, 1D CARDIOMYOPATHY, DILATED, 1DD CARDIOMYOPATHY, DILATED, 1E CARDIOMYOPATHY, DILATED, 1EE CARDIOMYOPATHY, DILATED, 1G CARDIOMYOPATHY, DILATED, ...
  7. ... hypocalcification type Genetic Testing Registry: Amelogenesis imperfecta, type 1E Genetic Testing Registry: Amelogenesis imperfecta, type IC Amelogenesis ...
  8. ... type 1D Genetic Testing Registry: Usher syndrome type 1E Genetic Testing Registry: Usher syndrome type 1F Genetic ...
  9. ... form of Charcot-Marie-Tooth disease called type 1E (CMT1E). CMT1E is associated with particular amino acid ...
  10. ... spot mutation in hereditary sensory and autonomic neuropathy 1E. Epigenetics. 2014 Aug;9(8):1184-93. doi: ...
previous · 1 · 2 · next