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Clinical Dysmorphology|October 1, 1995
Family studies in chromosome 22q11 deletion: further demonstration of phenotypic heterogeneityD De Silva, P Duffty, P Booth, et al.Neuropediatrics|April 25, 2000
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish familyW L Lee, C Biervert, K Hallmann, et al.Clinical Genetics|November 1, 1991
Apparent Fryns' syndrome and aneuploidy: evidence for a disturbance of the midline developmental fieldJ C Dean, D A Couzin, E S Gray, et al.Developmental Medicine and Child Neurology|March 13, 1999
Partial lipodystrophy presenting with myopathyS J Moore, I A Auchterlonie, G F Cole, et al.The Journal of Arthroplasty|December 1, 1995
Effects of hydroxyapatite tricalcium phosphate coating and intracancellous placement on bone ingrowth in titanium fibermetal implantsJ C Dean, C L Tisdel, V M Goldberg, et al.Journal of Medical Genetics|July 29, 1999
Fragile X syndrome with FMR1 and FMR2 deletionS J Moore, L Strain, G F Cole, et al.European Journal of Pediatrics|July 21, 1999
Chromosome 22q11 microdeletion and congenital heart disease--a survey in a paediatric populationD E Yong, P Booth, J Baruni, et al.Clinical Dysmorphology|October 1, 1995
A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?P D Turnpenny, D C De Silva, D W Gregory, et al.Journal of Medical Genetics|March 1, 1990
Cranial hemihypertrophy and neurodevelopmental prognosisJ C Dean, G F Cole, R E Appleton, et al.Journal of Medical Genetics|July 7, 2000
A clinical study of 57 children with fetal anticonvulsant syndromesS J Moore, P Turnpenny, A Quinn, et al.Pageof 12