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Journal of Medical Genetics|February 1, 1994
Partial trisomy 3q causing mild Cornelia de Lange phenotypeS E Holder, L M Grimsley, R W Palmer, et al.American Journal of Medical Genetics|October 1, 1991
Genetic and clinical heterogeneity of Stickler syndromeG M Vintiner, I K Temple, H R Middleton-Price, et al.The British Journal of Ophthalmology|October 1, 1991
Heterogeneity in dominant anterior segment malformationsG E Holmström, W P Reardon, M Baraitser, et al.Clinical Genetics|June 1, 1985
The FG syndrome: 7 new casesE M Thompson, M Baraitser, R H Lindenbaum, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1984
Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological reportM Baraitser, W Gooddy, A M Halliday, et al.Journal of Medical Genetics|December 1, 1987
Multiple pterygium syndrome: evolution of the phenotypeE M Thompson, D Donnai, M Baraitser, et al.Clinical Dysmorphology|April 1, 1994
A case with blepharophimosis resembling Ohdo syndromeJ A Maat-Kievit, P J Milla, J E Collins, et al.Clinical Dysmorphology|January 1, 1995
The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIC)W Reardon, R M Winter, L T Smith, et al.Neuropediatrics|October 1, 1996
A form of juvenile Batten disease with granular osmiophilic depositsB D Lake, E M Brett, S G BoydThe Journal of Pediatrics|July 1, 1989
Hypomelanosis of Ito: spectrum of the diseaseM T Glover, E M Brett, D J AthertonPageof 19