Angelman's syndromeCLAYTON-SMITH, J.Archives of disease in childhood. 1992, Vol 67, Num 7, pp 889-890, issn 0003-9888Article

Clinical research on Angelman syndrome in the United Kingdom : observations on 82 affected individualsCLAYTON-SMITH, J.American journal of medical genetics. 1993, Vol 46, Num 1, pp 12-15, issn 0148-7299Conference Paper

A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosisCLAYTON-SMITH, J; DONNAI, D.Journal of medical genetics. 1989, Vol 26, Num 5, pp 339-342, issn 0022-2593, 4 p.Article

Angelman syndrome: a review of the clinical and genetic aspectsCLAYTON-SMITH, J; LAAN, L.Journal of medical genetics. 2003, Vol 40, Num 2, pp 87-95, issn 0022-2593, 9 p.Article

Fetal valproate syndromeCLAYTON-SMITH, J; DONNAI, D.Journal of medical genetics. 1995, Vol 32, Num 9, pp 724-727, issn 0022-2593Article

A Further patient with the lethal type of Larsen syndromeCLAYTON-SMITH, J; DONNAI, D.Journal of medical genetics. 1988, Vol 25, Num 7, pp 499-500, issn 0022-2593Article

Evolving phenotype of Marfan's syndromeLIPSCOMB, K. J; CLAYTON-SMITH, J; HARRIS, R et al.Archives of disease in childhood. 1997, Vol 76, Num 1, pp 41-46, issn 0003-9888Article

Angelman syndromeCLAYTON-SMITH, J; PEMBREY, M. E.Journal of medical genetics. 1992, Vol 29, Num 6, pp 412-415, issn 0022-2593Article

Familial patent ductus arteriosus : A further case of CHAR syndromeSLAVOTINEK, A; CLAYTON-SMITH, J; SUPER, M et al.American journal of medical genetics. 1997, Vol 71, Num 2, pp 229-232, issn 0148-7299Article

Monozygotic twinning and Wiedemann-Beckwith syndromeCLAYTON-SMITH, J; READ, A. P; DONNAI, D et al.American journal of medical genetics. 1992, Vol 42, Num 4, pp 633-637, issn 0148-7299Article

Effects of fetal antiepileptic drug exposure: Outcomes at age 4.5 yearsMEADOR, K. J; BAKER, G. A; PRIVITERA, M et al.Neurology. 2012, Vol 78, Num 16, pp 1207-1214, issn 0028-3878, 8 p.Article

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric PhenotypesMEFFORD, H; SHARP, A; COLLINS, A et al.The New England journal of medicine. 2008, Vol 359, Num 16, pp 1685-1699, issn 0028-4793, 15 p.Article

Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene : a role for norrin in retinal angiogenesisBLACK, G. C. M; PERVEEN, R; BONSHEK, R et al.Human molecular genetics (Print). 1999, Vol 8, Num 11, pp 2031-2035, issn 0964-6906Article

Uniparental paternal disomy in Angelman's syndromeMALCOLM, S; CLAYTON-SMITH, J; NICHOLS, M et al.Lancet (British edition). 1991, Vol 337, Num 8743, pp 694-697, issn 0140-6736, 4 p.Article

Examination of fetuses after induced abortion for fetal abnormalityCLAYTON-SMITH, J; FARNDON, P. A; MCKEOWN, C et al.BMJ. British medical journal (International ed.). 1990, Vol 300, Num 6720, pp 295-297, issn 0959-8146Article

Spontaneous aortic rupture in a 22-year-oldMEMON, M. A; NICHOLSON, C. M; CLAYTON-SMITH, J et al.Postgraduate medical journal. 1996, Vol 72, Num 847, pp 311-313, issn 0032-5473Article

AUTISM SPECTRUM DISORDERS FOLLOWING IN UTERO EXPOSURE TO ANTIEPILEPTIC DRUGSBROMLEY, R. L; MAWER, G; CLAYTON-SMITH, J et al.Neurology. 2008, Vol 71, Num 23, pp 1923-1924, issn 0028-3878, 2 p.Article

Folate and Clefts of the Lip and Palate-A U.K.-Based Case-Control Study: Part I: Dietary and Supplemental FolateLITTLE, J; GILMOUR, M; MOSSEY, P. A et al.The Cleft palate-craniofacial journal. 2008, Vol 45, Num 4, pp 420-427, issn 1055-6656, 8 p.Article

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitusMACKAY, D. J. G; BOONEN, S. E; SHIELD, J. P. H et al.Human genetics. 2006, Vol 120, Num 2, pp 262-269, issn 0340-6717, 8 p.Article

Detection of a deletion of exons 8-16 of the UBE3A gene in familial Angelman syndrome using a semi-quantitative dosage PCR based assayBOYES, L; WALLACE, A. J; KRAJEWSKA-WALASEK, M et al.European journal of medical genetics. 2006, Vol 49, Num 6, pp 472-480, issn 1769-7212, 9 p.Article

Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeresSLAVOTINEK, A; ROSENBERG, M; DONNAI, D et al.Journal of medical genetics. 1999, Vol 36, Num 5, pp 405-411, issn 0022-2593Article

Angelman syndrome associated with a maternal 15q11-13 deletion of less than 200 kbBUXTON, J. L; CHAN, C-T. J; GILBERT, H et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1409-1413, issn 0964-6906Article

Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeCLAYTON-SMITH, J; DRISCOLL, D. J; WATERS, M. F et al.American journal of medical genetics. 1993, Vol 47, Num 5, pp 683-686, issn 0148-7299Article

Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and functionLACBAWAN, F; SOLOMON, B. D; FRYER, A et al.Journal of medical genetics. 2009, Vol 46, Num 6, pp 389-398, issn 0022-2593, 10 p.Article

FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic AbnormalityFANTES, J. A; BOLAND, E; HOLLOWAY, S et al.American journal of human genetics. 2008, Vol 82, Num 4, pp 916-926, issn 0002-9297, 11 p.Article