Results 1 -
10
of
14
for
1E -"5-phenyl-1-(3-phenyloxiran-2-yl)pent-1-en-3-one"
- ... Primary dilated cardiomyopathy Cardiomyopathy, dilated, 1a Cardiomyopathy, dilated, 1e Dilated cardiomyopathy National Organization for Rare Disorders (NORD) ...
- ... 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 ...
- ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Sjoholm AG, Jonsson G, Braconier ...
- ... 50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Citation on PubMed Corcia ...
- ... 8. doi: 10.1097/01.gim.0000245578.94312.1e. Citation on PubMed Voskoboinik I, Camakaris J. Menkes ...
- ... spot mutation in hereditary sensory and autonomic neuropathy 1E. Epigenetics. 2014 Aug;9(8):1184-93. doi: ...
- ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Krishnan V, Xu Y, Macon ...
- ... type 1C Genetic Testing Registry: Amelogenesis imperfecta type 1E Amelogenesis imperfecta National Organization for Rare Disorders (NORD) ...
- ... type 1D Genetic Testing Registry: Usher syndrome type 1E Genetic Testing Registry: Usher syndrome type 1F Genetic ...
- ... 5. doi: 10.1097/01.NURSE.0000279437.30155.1e. Citation on PubMed Gershman AJ, Mehta AC, Infeld ...