Search research articles
Contact Us
Filters
Showing results (121-130 of 133) with videos related to
Page
of 14
Sort By:
Lancet (London, England)
|
February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death
M J Bennett, F Allison, R J Pollitt, et al.
Annals of Clinical Biochemistry
|
March 1, 1994
Quality assessment of urinary organic acid analysis
J R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis
|
February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency
M J Bennett, F Allison, G W Lowther, et al.
Journal of Clinical Pathology
|
August 1, 1993
Familial hypercholesterolaemia: pilot study to identify children at risk
C J Taylor, S Olpin, J Rattenbury, et al.
Clinical Dysmorphology
|
January 1, 1994
Syndromes associated with trichothiodystrophy
J L Tolmie, D de Berker, R Dawber, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of glutathione synthase deficiency
N 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 deficiency
Y 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 II
N 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 outcome
R J Pollitt, A Green, C J McCabe, et al.
Progress in Medicinal Chemistry
|
January 1, 1975
The medicinal chemistry of lithium
E Bailey, P A Bond, B A Brooks, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 133) with videos related to
Sort By:
Page
of 14
Lancet (London, England)
|
February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death
M J Bennett, F Allison, R J Pollitt, et al.
Annals of Clinical Biochemistry
|
March 1, 1994
Quality assessment of urinary organic acid analysis
J R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis
|
February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency
M J Bennett, F Allison, G W Lowther, et al.
Journal of Clinical Pathology
|
August 1, 1993
Familial hypercholesterolaemia: pilot study to identify children at risk
C J Taylor, S Olpin, J Rattenbury, et al.
Clinical Dysmorphology
|
January 1, 1994
Syndromes associated with trichothiodystrophy
J L Tolmie, D de Berker, R Dawber, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of glutathione synthase deficiency
N 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 deficiency
Y 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 II
N 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 outcome
R J Pollitt, A Green, C J McCabe, et al.
Progress in Medicinal Chemistry
|
January 1, 1975
The medicinal chemistry of lithium
E Bailey, P A Bond, B A Brooks, et al.
Page
of 14