S Malcolm

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

Jess Tyson, S. Bellman, Christopher Wren et al. · Human Molecular Genetics · 1997 · 312 citations · Full text

Molecular mechanisms in Angelman syndrome: a survey of 93 patients.

Christopher T. Chan, Jill Clayton‐Smith, Xingbo Cheng et al. · Journal of Medical Genetics · 1993 · 145 citations · Full text

Down Syndrome, Clinical Disorders, Cytogenetic Analysis +11

Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome

M. OIdridge, Andrew O.M. Wilkie, S.F. SIaney et al. · Human Molecular Genetics · 1995 · 142 citations

Sclerostin, Human Growth, Genetics +21

Guidelines for Research Involving Recombinant DNA Molecules

S Malcolm · Journal of Medical Genetics · 1978 · 134 citations · Full text

Cytogenetics, Genetics, Molecular Biology +19

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome

Daniel Kelberman, Jess Tyson, David Chandler et al. · Human Genetics · 2001 · 131 citations

Down Syndrome, Developmental Anomaly, Developmental Biology +10