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Clinical Genetics|September 1, 1990
Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?W Reardon, I K Temple, B Jones, et al.Clinical Genetics|August 1, 1986
A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infectionJ Burn, H T Wickramasinghe, B Harding, et al.Journal of Medical Genetics|June 1, 1984
Orofaciodigital syndrome with mesomelic limb shorteningJ Burn, C Dezateux, C M Hall, et al.Clinical Genetics|March 1, 1991
Atypical facio-scapulo-humeral muscular dystrophy--a counselling dilemmaW Reardon, I K Temple, G Harwood, et al.Journal of Medical Genetics|September 1, 1991
Sibs with mental retardation, supraorbital sclerosis, and metaphyseal dysplasia: frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome?W Reardon, C M Hall, M J Dillon, et al.Journal of Medical Genetics|April 1, 1985
The clinical features of the Cohen syndrome: further case reportsC North, M A Patton, M Baraitser, et al.Archives of Disease in Childhood|September 1, 1990
The iris in Williams syndromeG Holmström, G Almond, K Temple, et al.Clinical Dysmorphology|April 1, 1993
Congenital cataract, microphthalmia and septal heart defect in two generations: a new syndrome?A O Wilkie, D Taylor, P J Scambler, et al.Journal of Medical Genetics|June 1, 1990
Proteus syndrome: report of a case with severe brain impairment and fatal courseR Rizzo, L Pavone, G Sorge, et al.Clinical Genetics|September 1, 1980
Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further caseR M Winter, D M Swallow, M Baraitser, et al.Pageof 19