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European Journal of Pediatrics|February 1, 1984
Ornithine carbamoyl transferase deficiency: a neuropathological studyB N Harding, J V Leonard, M ErdohaziNeuropathology and Applied Neurobiology|April 1, 1991
Propionic acidaemia: a neuropathological study of two patients presenting in infancyB N Harding, J V Leonard, M ErdohaziJournal of Medical Genetics|April 1, 1987
A girl with the Weaver syndromeE M Thompson, S Hill, J V Leonard, et al.Archives of Disease in Childhood|April 1, 1991
Nesidioblastosis: evidence for autosomal recessive inheritanceD A Woolf, J V Leonard, R C Trembath, et al.Journal of Medical Genetics|December 1, 1985
Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probeM E Pembrey, J M Old, J V Leonard, et al.Bailliere'S Clinical Obstetrics and Gynaecology|September 1, 1987
The impact of DNA analysis on fetal diagnosisM E PembreyJournal of Inherited Metabolic Disease|January 1, 1986
Applications and limitations of direct DNA analysis in genetic predictionM E PembreyHuman Genetics|September 1, 1986
Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting malesR M Winter, M E PembreyJournal of Child Neurology|October 1, 1990
Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): a personal reviewB N HardingJournal of Medical Genetics|March 1, 1988
A reappraisal of the CHARGE associationC A Oley, M Baraitser, D B GrantPageof 30