Showing 1 - 3 results of 3 for search 'Neil Ingham', query time: 0.01s Refine Results
  1. 1
    Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media.

    Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media. by Stephanie Kuhn, Neil Ingham, Selina Pearson, Susan M Gribble, Stephen Clayton, Karen P Steel, Walter Marcotti

    Published 2012-01-01
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  2. 2
    Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

    Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss. by Jing Chen, Neil Ingham, John Kelly, Shalini Jadeja, David Goulding, Johanna Pass, Vinit B Mahajan, Stephen H Tsang, Anastasia Nijnik, Ian J Jackson, Jacqueline K White, Andrew Forge, Daniel Jagger, Karen P Steel

    Published 2014-10-01
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  3. 3
    Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene.

    Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene. by Simon Maguire, Jeanne Estabel, Neil Ingham, Selina Pearson, Edward Ryder, Damian M Carragher, Nicolas Walker, Sanger MGP Slc25a21 Project Team, James Bussell, Wai-In Chan, Thomas M Keane, David J Adams, Cheryl L Scudamore, Christopher J Lelliott, Ramiro Ramírez-Solis, Natasha A Karp, Karen P Steel, Jacqueline K White, Anna-Karin Gerdin

    Published 2014-01-01
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