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Matthew J Scanlan

  1. "Cell Press"
Formats
  1. Meeting Abstract (1)
Years
  1. 2000 (1)
Publications
  1. American Journal of Human Genetics (1)
Publishers
  1. Cell Press (1)

Results (1)

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  • A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness, identifies the gene for Usher syndrome type 1C
    Meeting Abstract

    Bitner-Glindzicz, M.; Rutland, P.; Lindley, K. J.; Blaydon, D.; Smith, V. V.; Milla, P. J.; Hussain, K.; Furth-Lavi, J.; Cosgrove, K. E.; Shepherd, R. M.; more...
    American Journal of Human Genetics (2000)

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