Results 1 -
10
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11
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1E -"4-hydroxy-1-(4-methoxyphenyl)pent-1-en-3-one"
- ... 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: ...
- ... 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 ...
- Usher Syndrome/Learn More ... Usher Syndrome ... A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information ...
- ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Sjöholm AG, Jönsson G, Braconier ...
- ... 34. doi: 10.1097/01.md.0000152371.22747.1e. Citation on PubMed Krishnan V, Xu Y, Macon ...
- ... CARDIOMYOPATHY, DILATED, 1D CARDIOMYOPATHY, DILATED, 1DD CARDIOMYOPATHY, DILATED, 1E CARDIOMYOPATHY, DILATED, 1EE CARDIOMYOPATHY, DILATED, 1G CARDIOMYOPATHY, DILATED, ...
- ... hypocalcification type Genetic Testing Registry: Amelogenesis imperfecta, type 1E Genetic Testing Registry: Amelogenesis imperfecta, type IC Amelogenesis ...
- ... type 1D Genetic Testing Registry: Usher syndrome type 1E Genetic Testing Registry: Usher syndrome type 1F Genetic ...
- ... form of Charcot-Marie-Tooth disease called type 1E (CMT1E). CMT1E is associated with particular amino acid ...
- ... spot mutation in hereditary sensory and autonomic neuropathy 1E. Epigenetics. 2014 Aug;9(8):1184-93. doi: ...