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Results 1 - 10 of 14 for 1E -"1-(4-methoxyphenyl)pent-1-en-3-ol"
  1. ... dementia syndrome Hereditary sensory and autonomic neuropathy type 1E National Organization for Rare Disorders (NORD) ClinicalTrials.gov ... spot mutation in hereditary sensory and autonomic neuropathy 1E. Epigenetics. 2014 Aug;9(8):1184-93. doi: ...
  2. ... Genetic Testing Registry: Primary dilated cardiomyopathy Cardiomyopathy, dilated, 1e Dilated cardiomyopathy Cardiomyopathy, dilated, 1a National Organization for ...
  3. ... 1D Genetic Testing Registry: Congenital stationary night blindness 1E Genetic Testing Registry: Congenital stationary night blindness 1F ... CONGENITAL NONPROGRESSIVE; CRSD NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E; CSNB1E NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F ...
  4. ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Sjoholm AG, Jonsson G, Braconier ...
  5. ... 50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Citation on PubMed Corcia ...
  6. ... 8. doi: 10.1097/01.gim.0000245578.94312.1e. Citation on PubMed Voskoboinik I, Camakaris J. Menkes ...
  7. ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Krishnan V, Xu Y, Macon ...
  8. ... type 1C Genetic Testing Registry: Amelogenesis imperfecta type 1E Amelogenesis imperfecta National Organization for Rare Disorders (NORD) ...
  9. ... type 1D Genetic Testing Registry: Usher syndrome type 1E Genetic Testing Registry: Usher syndrome type 1F Genetic ...
  10. ... 5. doi: 10.1097/01.NURSE.0000279437.30155.1e. Citation on PubMed Gershman AJ, Mehta AC, Infeld ...
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