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Citation: Emr. De Leenheer et al., Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13), ARCH OTOLAR, 127(1), 2001, pp. 13-17

Authors: Van Laer, L Coucke, P Mueller, RF Caethoven, G Flothmann, K Prasad, SD Chamberlin, GP Houseman, M Taylor, GR Van de Heyning, CM Fransen, E Rowland, J Cucci, RA Smith, RJH Van Camp, G

Citation: L. Van Laer et al., A common founder for the 35deIG GJB2 gene mutation in connexin 26 hearing impairment, J MED GENET, 38(8), 2001, pp. 515-518

Authors: McGuirt, WT Prasad, SD Griffith, AJ Kunst, HPM Green, GE Shpargel, KB Runge, C Huybrechts, C Mueller, RF Lynch, E King, MC Brunner, HG Cremers, CWRJ Takanosu, M Li, SW Arita, M Mayne, R Prockop, DJ Van Camp, G Smith, RJH

Citation: Wt. Mcguirt et al., Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13), NAT GENET, 23(4), 1999, pp. 413-419

Authors: Prasad, SD

Citation: Sd. Prasad, Looking for gold in Langmuir's data: Surface heterogeneity identification through pressure derivatives, LANGMUIR, 15(18), 1999, pp. 5722-5732