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Results of search for 'au:"Hopkinson, D A"', page 6 of 9
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Authors
Abbott, C M
Adinolfi, A
Barker, R F
Bobrow, M
Cook, P J
Corney, G
Edwards, Y H
HARRIS, H
HOPKINSON, D A
Harris, H
Hopkinson, D A
Johnson, P H
Lovegrove, J U
Mieli-Vergani, G
Povey, S
Putt, W
Robson, E B
Smith, M
Swallow, D M
Whitehouse, D B
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Animals
Chromosome Mapping
Electrophoresis
Electrophoresis, Starch Gel
Erythrocytes
Female
Genes
Genetic Variation
Humans
Isoenzymes
Liver
Male
Phenotype
Phosphoglucomutase
Polymorphism, Genetic
analysis
blood
enzymology
genetics
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English
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101.
Pyrimidine 5'-nucleotidase activity in normal and deficient human lymphoblastoid cells.
[electronic resource]
by
Hopkinson, D A
Swallow, D M
Marinaki, A
Harley, E H
Producer:
19910110
In:
Journal of inherited metabolic disease
vol. 13
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102.
Electrophoresis of human l-glutamate dehydrogenase: tissue distribution and preliminary population survey.
[electronic resource]
by
Nelson, R L
Povey, M S
Hopkinson, D A
Harris, H
Producer:
19770512
In:
Biochemical genetics
vol. 15
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103.
Isolation of a cDNA clone for the human muscle specific carbonic anhydrase, CAIII.
[electronic resource]
by
Lloyd, J C
Isenberg, H
Hopkinson, D A
Edwards, Y H
Producer:
19860109
In:
Annals of human genetics
vol. 49
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104.
Red cell adenosine deaminase (ADA) polymorphism in Southern Africa, with special reference to ADA deficiency among the !Kung.
[electronic resource]
by
Jenkins, T
Lane, A B
Nurse, G T
Hopkinson, D A
Producer:
19791026
In:
Annals of human genetics
vol. 42
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105.
Interstitial deletion of chromosome band 13q14 associated with squamous cell carcinoma.
[electronic resource]
by
Fitchett, M
Downing, R G
Hopkinson, D A
Bayley, A C
Producer:
19850122
In:
Journal of medical genetics
vol. 21
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106.
Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1).
[electronic resource]
by
Yip, S P
Putt, W
Hopkinson, D A
Whitehouse, D B
Producer:
20000504
In:
Annals of human genetics
vol. 63
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107.
Identification of alcohol dehydrogenase and aldehyde dehydrogenase isoenzymes in human liver biopsy specimens.
[electronic resource]
by
Ricciardi, B R
Saunders, J B
Williams, R
Hopkinson, D A
Producer:
19830708
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 130
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108.
Rhodanese isozymes in human tissues.
[electronic resource]
by
Whitehouse, D B
Pilz, A J
Porta, G
Hopkinson, D A
Producer:
19881114
In:
Annals of human genetics
vol. 52
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109.
Hepatic ADH and ALDH isoenzymes in different racial groups and in chronic alcoholism.
[electronic resource]
by
Ricciardi, B R
Saunders, J B
Williams, R
Hopkinson, D A
Producer:
19831220
In:
Pharmacology, biochemistry, and behavior
vol. 18 Suppl 1
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110.
Evidence for a distinct deoxypyrimidine 5'-nucleotidase in human tissues.
[electronic resource]
by
Hopkinson, D A
Swallow, D M
Turner, V S
Aziz, I
Producer:
19840606
In:
Advances in experimental medicine and biology
vol. 165 Pt A
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111.
Acetylator phenotypes in Papua New Guinea.
[electronic resource]
by
Penketh, R J
Gibney, S F
Nurse, G T
Hopkinson, D A
Producer:
19830623
In:
Journal of medical genetics
vol. 20
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112.
Analysis of genetic variation in two human thyroxine-binding plasma proteins by immunodetection after isoelectric focusing.
[electronic resource]
by
Whitehouse, D B
Hopkinson, D A
Hill, A V
Bowden, D K
Producer:
19860109
In:
Annals of human genetics
vol. 49
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113.
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybrids.
[electronic resource]
by
Hopkinson, D A
Povey, S
Solomon, E
Bobrow, M
Gormley, I P
Producer:
19761223
In:
Cytogenetics and cell genetics
vol. 16
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114.
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybrids.
[electronic resource]
by
Hopkinson, D A
Povey, S
Solomon, E
Bobrow, M
Gormiley, I P
Producer:
19770611
In:
Birth defects original article series
vol. 12
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115.
Antigenic analysis of the major human phosphoglucomutase isozymes: PGM1, PGM2, PGM3 and PGM4.
[electronic resource]
by
Drago, G A
Hopkinson, D A
Westwood, S A
Whitehouse, D B
Producer:
19920723
In:
Annals of human genetics
vol. 55
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116.
A COL3A1 glycine 1006 to glutamic acid substitution in a patient with Ehlers-Danlos syndrome type IV detected by denaturing gradient gel electrophoresis.
[electronic resource]
by
Johnson, P H
Richards, A J
Pope, F M
Hopkinson, D A
Producer:
19921116
In:
Journal of inherited metabolic disease
vol. 15
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117.
Inosine triphosphate pyrophosphohydrolase deficiency in a kindred with adenosine deaminase deficiency.
[electronic resource]
by
Duley, J A
Simmonds, H A
Hopkinson, D A
Levinsky, R J
Producer:
19900927
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 188
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118.
Adenosine deaminase activity in a series of 19 patients with the Diamond-Blackfan syndrome.
[electronic resource]
by
Whitehouse, D B
Hopkinson, D A
Pilz, A J
Arredondo, F X
Producer:
19860805
In:
Advances in experimental medicine and biology
vol. 195 Pt A
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119.
Rhodanese isozymes in three subjects with Leber's optic neuropathy.
[electronic resource]
by
Whitehouse, D B
Poole, C J
Kind, P R
Hopkinson, D A
Producer:
19890327
In:
Journal of medical genetics
vol. 26
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120.
The detection and differentiation of the products of the human carbonic anhydrase loci, CAI and CAII using fluorogenic substrates.
[electronic resource]
by
Hopkinson, D A
Coppock, J S
Mühlemann, M F
Edwards, Y H
Producer:
19751211
In:
Annals of human genetics
vol. 38
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