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Results 1 - 6 of 6 for 3D
  1. Hereditary neuralgic amyotrophy 
    ... 3Chtml%3E%3Chead%3E%0A%3Cmeta+http-equiv%3D%22content-type%22+content%3D%22text%2Fhtml%3Bcharset%3Dutf-8%22%3E%0A% ... 3E%0A%3C%2Fhead%3E%0A%3Cbody+text%3D%23000000+bgcolor%3D%23ffffff%3E%0A%3Ch1%3EError% ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
  2. Hereditary xanthinuria 
    ... 3Chtml%3E%3Chead%3E%0A%3Cmeta+http-equiv%3D%22content-type%22+content%3D%22text%2Fhtml%3Bcharset%3Dutf-8%22%3E%0A% ... 3E%0A%3C%2Fhead%3E%0A%3Cbody+text%3D%23000000+bgcolor%3D%23ffffff%3E%0A%3Ch1%3EError% ...
    https://medlineplus.gov/genetics/condition/hereditary-xanthinuria - Genetics
  3. Hirschsprung disease 
    ... Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical ...
    https://medlineplus.gov/genetics/condition/hirschsprung-disease - Genetics
  4. Parkinson's disease 
    ... 9. doi: 10.1097/01.wco.0000170951.08924.3d. Citation on PubMed Hardy J, Cai H, Cookson ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  5. Spastic paraplegia type 11 
    ... 9. doi: 10.1212/01.wnl.0000294327.66106.3d. Epub 2008 Mar 12. Citation on PubMed or ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-11 - Genetics
  6. SRD5A3-congenital disorder of glycosylation 
    ... Triki C, Alimi AM, Masmoudi S. SRD5A3-CDG: 3D structure modeling, clinical spectrum, and computer-based dysmorphic ...
    https://medlineplus.gov/...d5a3-congenital-disorder-of-glycosylation - Genetics