P F Benson|A H Fensom|P E Polani - JoVE Visualize

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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 Benson

The British Journal of Ophthalmology|August 1, 1976

Corneal clouding in GM1-generalized gangliosidosisA Babarik, P F Benson, A H Fensom

British Medical Journal|November 16, 1974

Prenatal diagnosis of galactosaemiaA H Fensom, P F Benson, S Blunt

British Journal of Obstetrics and Gynaecology|June 1, 1980

Amniotic fluid acetylcholinesterase and prenatal diagnosisM J Seller, K J Cole, A H Fensom, et al.

Clinica 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 Baker

Prenatal 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.

Birth Defects Original Article Series|January 1, 1976

Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studiesP F Benson, S P Brown, J Cree, et al.

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Showing results (1-10 of 94) with videos related to

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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 Benson

The British Journal of Ophthalmology|August 1, 1976

Corneal clouding in GM1-generalized gangliosidosisA Babarik, P F Benson, A H Fensom

British Medical Journal|November 16, 1974

Prenatal diagnosis of galactosaemiaA H Fensom, P F Benson, S Blunt

British Journal of Obstetrics and Gynaecology|June 1, 1980

Amniotic fluid acetylcholinesterase and prenatal diagnosisM J Seller, K J Cole, A H Fensom, et al.

Clinica 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 Baker

Prenatal 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.

Birth Defects Original Article Series|January 1, 1976

Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studiesP F Benson, S P Brown, J Cree, et al.

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