S Malcolm

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge et al. · Nature Genetics · 1995 · 937 citations

Life Sciences, Genetics, Molecular Genetics +7

Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene <i>POU3F4</i>

Yvette J.M. de Kok, Silvère M. van der Maarel, Maria Bitner‐Glindzicz et al. · Science · 1995 · 449 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Uniparental paternal disomy in Angelman's syndrome

S Malcolm, Jill Clayton‐Smith, M. Nichols et al. · The Lancet · 1991 · 330 citations

Life Sciences, Genetics, Cytogenetics +6

Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization.

S Malcolm, Paul J.R. Barton, Clifton N. Murphy et al. · Proceedings of the National Academy of Sciences · 1982 · 248 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Resistance to hygromycin B

Clive Waldron, E. Murphy, Jean L. Roberts et al. · Plant Molecular Biology · 1985 · 209 citations

Life Sciences, Microbiology, Antimicrobial Pharmacotherapy +7