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Journal Abstract Search

162 related items for PubMed ID: 27617158

  • 1. Fanconi-Bickel Syndrome: Two Pakistani Patients Presenting with Hypophosphatemic Rickets.
    Afroze B, Chen M.
    J Pediatr Genet; 2016 Sep; 5(3):161-6. PubMed ID: 27617158
    [Abstract] [Full Text] [Related]

  • 2. An Indian girl with Fanconi-Bickel syndrome without SLC2A2 gene mutation.
    Dayal D, Dekate P, Sharda S, Das A, Attri S.
    J Pediatr Genet; 2013 Jun; 2(2):109-12. PubMed ID: 27625848
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  • 3. A Fanconi-Bickel syndrome patient with a novel mutation and accompanying situs inversus totalis.
    Taştemel-Öztürk T, Bilginer-Gürbüz B, Tekşam Ö, Sivri S.
    Turk J Pediatr; 2017 Jun; 59(6):693-695. PubMed ID: 30035403
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  • 4. A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome.
    Simşek E, Savaş-Erdeve S, Sakamoto O, Doğanci T, Dallar Y.
    Turk J Pediatr; 2009 Jun; 51(2):166-8. PubMed ID: 19480329
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  • 5. Segregation of a novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi-Bickel syndrome family.
    Abbasi F, Azizi F, Javaheri M, Mosallanejad A, Ebrahim-Habibi A, Ghafouri-Fard S.
    Gene; 2015 Feb 15; 557(1):103-5. PubMed ID: 25523092
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  • 6. Hypophosphatemic rickets: presenting features of fanconi-bickel syndrome.
    Roy M, Bose K, Paul DK, Anand P.
    Case Rep Pathol; 2011 Feb 15; 2011():314696. PubMed ID: 22937383
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  • 14. Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering.
    Al-Haggar M, Sakamoto O, Shaltout A, Al-Hawari A, Wahba Y, Abdel-Hadi D.
    Clin Exp Nephrol; 2012 Aug 15; 16(4):604-10. PubMed ID: 22350464
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  • 17. Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.
    Pogoriler J, O'Neill AF, Voss SD, Shamberger RC, Perez-Atayde AR.
    Pediatr Dev Pathol; 2018 Aug 15; 21(1):84-90. PubMed ID: 28382841
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  • 19. Fanconi-Bickel syndrome.
    Karande S, Kumbhare N, Kulkarni M.
    Indian Pediatr; 2007 Mar 15; 44(3):223-5. PubMed ID: 17413201
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