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Results 1 - 4 of 4 for Pearson syndrome
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  1. SLC2A1 gene 
    ... 10.1530/eje.0.1500627. Citation on PubMed Pearson TS, Akman C, Hinton VJ, Engelstad K, De Vivo DC. Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS). Curr Neurol Neurosci Rep. 2013 Apr; ...
    https://medlineplus.gov/genetics/gene/slc2a1 - Genetics
  2. YWHAE gene 
    ... Hunter JV, Sparagana S, Lagoe E, Fong CT, Pearson M, Doco-Fenzy M, Landais E, Mozelle M, Chinault AC, Patel A, Bacino CA, Sahoo T, Kang SH, Cheung SW, Lupski JR, Stankiewicz P. Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial ...
    https://medlineplus.gov/genetics/gene/ywhae - Genetics
  3. IGF2 gene 
    ... PubMed Eggermann T. Silver-Russell and Beckwith-Wiedemann syndromes: ... CA, Ohlsson R, Andraos R, Pearson MA, Sharov AA, Longo DL, Ko MS, Levchenko ...
    https://medlineplus.gov/genetics/gene/igf2 - Genetics
  4. LHX1 gene 
    ... Küster-Hauser syndrome in people with 17q12 deletion syndrome. More About This Health Condition ... A, Shen J, Li C, Roeder E, Cox S, Karaviti L, Pearson M, Kang SH, Sahoo T, Lalani SR, Stankiewicz ...
    https://medlineplus.gov/genetics/gene/lhx1 - Genetics