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Clinica Chimica Acta; International Journal of Clinical Chemistry|July 23, 1975
Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemiaA H Fensom, P F BensonThe British Journal of Ophthalmology|August 1, 1976
Corneal clouding in GM1-generalized gangliosidosisA Babarik, P F Benson, A H FensomDevelopmental Medicine and Child Neurology|February 1, 1975
The effect of dextran infusions on glycosaminoglycan excretion in the Sanfilippo syndromeM F Dean, P F Benson, H MuirBritish Medical Journal|November 16, 1974
Prenatal diagnosis of galactosaemiaA H Fensom, P F Benson, S BluntClinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1978
A rapid method for assay of branched-chain keto acid decarboxylation in cultured cells and its application to prenatal diagnosis of maple syrup urine diseaseA H Fensom, P F Benson, J E BakerFEBS Letters|April 24, 1990
Intra- and extraluminal sarcoplasmic reticulum membrane regulatory sites for Ca2(+)-induced Ca2+ releaseT E Nelson, K E NelsonPrenatal Diagnosis|July 1, 1983
Prenatal exclusion of late infantile metachromatic leucodystrophy in a late-presenting pregnancy by assay of fetal leucocytesC H Rodeck, A H Fensom, P F Benson, et al.Clinical Genetics|November 1, 1979
Prenatal diagnosis of galactosaemia in six pregnancies -- possible complications with rare alleles of the galactose 1-phosphate uridyl transferase locusP F Benson, N J Brandt, E Christensen, et al.Journal of Inherited Metabolic Disease|January 1, 1980
Fibroblast alpha-galactosidase A activity for identification of Fabry's disease heterozygotesA H Fensom, P F Benson, A R Grant, et al.Clinical Genetics|November 1, 1979
Lumbar kyphosis in Hunter's disease (MPS ii)P F Benson, L R Button, A H Fensom, et al.Pageof 317