M Baraitser

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes

Paul Rutland, Louise J. Pulleyn, William Reardon et al. · Nature Genetics · 1995 · 457 citations

Life Sciences, Genetics, Molecular Genetics +7

X-linked recessive bulbospinal neuronopathy: a report of ten cases.

A E Harding, P. K. Thomas, M Baraitser et al. · Journal of Neurology Neurosurgery & Psychiatry · 1982 · 245 citations · Full text

Medicine, Neurology, Neuroscience +15

Genetic Basis of the Epilepsies

M Baraitser · Journal of Neurology Neurosurgery & Psychiatry · 1982 · 183 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Focal dermal hypoplasia (Goltz syndrome).

I. Karen Temple, P MacDowall, M Baraitser et al. · Journal of Medical Genetics · 1990 · 131 citations · Full text

Medicine, Dermatology, Genetics +11

Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome)

Christine Oley, M Baraitser · Journal of Medical Genetics · 1988 · 128 citations · Full text

Life Sciences, Dermatology, Genetics +9