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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

M. Bitner-Glindzicz

Department of Clinical and Molecular Genetics

Institute of Child Health

and Great Ormond Street Hospital for Children NHS Trust




Name/email consistency: high



  • Department of Clinical and Molecular Genetics, Institute of Child Health, and Great Ormond Street Hospital for Children NHS Trust, London, UK. 2000 - 2010


  1. Aminoglycoside-induced deafness during treatment of acute leukaemia. Bitner-Glindzicz, M., Osei-Lah, V., Colvin, I., Sirimanna, T., Lucas, D., Mac Ardle, B., Webb, D., Shankar, A., Kingston, J., Jenkins, L., Rahman, S. Arch. Dis. Child. (2010) [Pubmed]
  2. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene. Bitner-Glindzicz, M., Lindley, K.J., Rutland, P., Blaydon, D., Smith, V.V., Milla, P.J., Hussain, K., Furth-Lavi, J., Cosgrove, K.E., Shepherd, R.M., Barnes, P.D., O'Brien, R.E., Farndon, P.A., Sowden, J., Liu, X.Z., Scanlan, M.J., Malcolm, S., Dunne, M.J., Aynsley-Green, A., Glaser, B. Nat. Genet. (2000) [Pubmed]
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