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R J Pollitt

Showing results (121-130 of 133) with videos related to

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Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, et al.
Annals of Clinical Biochemistry|March 1, 1994
Quality assessment of urinary organic acid analysisJ R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyM J Bennett, F Allison, G W Lowther, et al.
Journal of Clinical Pathology|August 1, 1993
Familial hypercholesterolaemia: pilot study to identify children at riskC J Taylor, S Olpin, J Rattenbury, et al.
Clinical Dysmorphology|January 1, 1994
Syndromes associated with trichothiodystrophyJ L Tolmie, D de Berker, R Dawber, et al.
Prenatal Diagnosis|June 1, 1994
Prenatal diagnosis of glutathione synthase deficiencyN J Manning, N P Davies, S E Olpin, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyY Matsubara, K Narisawa, S Miyabayashi, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type IIN J Manning, J R Bonham, M Downing, et al.
Health Technology Assessment (Winchester, England)|January 1, 1997
Neonatal screening for inborn errors of metabolism: cost, yield and outcomeR J Pollitt, A Green, C J McCabe, et al.
Progress in Medicinal Chemistry|January 1, 1975
The medicinal chemistry of lithiumE Bailey, P A Bond, B A Brooks, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, et al.
Annals of Clinical Biochemistry|March 1, 1994
Quality assessment of urinary organic acid analysisJ R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyM J Bennett, F Allison, G W Lowther, et al.
Journal of Clinical Pathology|August 1, 1993
Familial hypercholesterolaemia: pilot study to identify children at riskC J Taylor, S Olpin, J Rattenbury, et al.
Clinical Dysmorphology|January 1, 1994
Syndromes associated with trichothiodystrophyJ L Tolmie, D de Berker, R Dawber, et al.
Prenatal Diagnosis|June 1, 1994
Prenatal diagnosis of glutathione synthase deficiencyN J Manning, N P Davies, S E Olpin, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyY Matsubara, K Narisawa, S Miyabayashi, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type IIN J Manning, J R Bonham, M Downing, et al.
Health Technology Assessment (Winchester, England)|January 1, 1997
Neonatal screening for inborn errors of metabolism: cost, yield and outcomeR J Pollitt, A Green, C J McCabe, et al.
Progress in Medicinal Chemistry|January 1, 1975
The medicinal chemistry of lithiumE Bailey, P A Bond, B A Brooks, et al.
Pageof 14