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Results 61 - 68 of 68 for Wilson sign
  1. Blepharophimosis, ptosis, and epicanthus inversus syndrome 
    ... Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel ...
    https://medlineplus.gov/...s-ptosis-and-epicanthus-inversus-syndrome - Genetics
  2. Mitochondrial membrane protein-associated neurodegeneration 
    ... Foulds NC, Hammans SR, Desguerre I, Rodriguez D, Wilson C, Diedrich A, Green S, Tran H, Reese ...
    https://medlineplus.gov/...rane-protein-associated-neurodegeneration - Genetics
  3. SATB2-associated syndrome 
    ... Steinraths M, Matthews A, Smith WE, Sun A, Wilson LC, Brain C, Allgove J, Jacobs B, Fish ...
    https://medlineplus.gov/genetics/condition/satb2-associated-syndrome - Genetics
  4. Steatocystoma multiplex 
    ... 1998.02413.x. Citation on PubMed Gass JK, Wilson NJ, Smith FJ, Lane EB, McLean WH, Rytina ...
    https://medlineplus.gov/genetics/condition/steatocystoma-multiplex - Genetics
  5. Fuchs endothelial dystrophy 
    ... KH, Mootha VV, Patel SV, Gregory SG, Bailey-Wilson JE, Price MO, Price FW Jr, Craig JE, ...
    https://medlineplus.gov/.../condition/fuchs-endothelial-dystrophy - Genetics
  6. Hyperferritinemia-cataract syndrome 
    ... DG, Manova-Todorova K, Farmer J, Lobmayr L, Wilson RB, Eagle RC Jr, St Pierre TG, Stambolian ...
    https://medlineplus.gov/.../hyperferritinemia-cataract-syndrome - Genetics
  7. Smith-Kingsmore syndrome 
    ... Lupski JR, Shendure J, Saneto RP, Novotny EJ, Wilson CJ, Sellers WR, Morrissey M, Hevner RF, Ojemann ...
    https://medlineplus.gov/genetics/condition/smith-kingsmore-syndrome - Genetics
  8. Congenital diaphragmatic hernia 
    ... Erlich JM, Mannisto S, Urban Z, Heikinheimo M, Wilson DB. Molecular genetics of congenital diaphragmatic defects. Ann ...
    https://medlineplus.gov/.../congenital-diaphragmatic-hernia - Genetics
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