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The Quarterly Journal of Medicine|May 1, 1990
The neurological complications of Anderson-Fabry disease (alpha-galactosidase A deficiency)--investigation of symptomatic and presymptomatic patientsS H Morgan, P Rudge, S J Smith, et al.Clinical Genetics|December 1, 1980
Osteopathia striata with cranial sclerosis: Highly variable expression within a family including cleft palate in two neonatal casesR M Winter, Crawfurd Md'A, H B Meire, et al.American Journal of Medical Genetics|December 1, 1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13L Brueton, S M Huson, R M Winter, et al.Journal of Medical Genetics|November 1, 1987
Fetal valproate syndrome: is there a recognisable phenotype?R M Winter, D Donnai, J Burn, et al.Journal of Medical Genetics|February 1, 1988
A combinatorial method for grouping cases with multiple malformationsR M Winter, R D Clark, K Ashley, 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.Journal of Medical Genetics|December 1, 1989
Unknown syndrome: microcephaly, hypoplastic nose, exophthalmos, gum hyperplasia, cleft palate, low set ears, and osteosclerosisJ Raine, R M Winter, A Davey, et al.American Journal of Medical Genetics|October 1, 1993
Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2W Reardon, S P McManus, D Summers, 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.Lancet (London, England)|November 24, 1984
First-trimester diagnosis of Lesch-Nyhan syndromeD A Gibbs, I R McFadyen, M D Crawfurd, et al.Pageof 19