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Results of search for 'au:"Sheppard, D M"', page 1 of 2
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Authors
Amick, B C
Bradshaw, J A
Bradshaw, J L
Bull, M
Clay, F
Collie, A
Cooper, N R
Crawfurd, M D
Croft, R J
Elder, G H
Fisher, R A
Fitzgerald, P B
Lawler, S D
Lee, P
Mattingley, J B
Segrave, R A
Sheer, D
Sheppard, D M
Thomson, R H
Tovey, J A
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Adolescent
Adult
Alpha Rhythm
Animals
Attention
Attention Deficit Disorder with Hyperactivity
Carboxy-Lyases
Cell Line
Child
Female
Functional Laterality
Humans
Karyotyping
Liver
Male
Pregnancy
enzymology
genetics
physiology
physiopathology
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English
Your search returned 25 results.
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1.
Immunoreactive uroporphyrinogen decarboxylase is unchanged in porphyria caused by TCDD and hexachlorobenzene.
[electronic resource]
by
Elder, G H
Sheppard, D M
Producer:
19830311
In:
Biochemical and biophysical research communications
vol. 109
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2.
The neurodevelopmental frontostriatal disorders: evolutionary adaptiveness and anomalous lateralization.
[electronic resource]
by
Bradshaw, J L
Sheppard, D M
Producer:
20000816
In:
Brain and language
vol. 73
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3.
Laboratory instrument for measuring electrical conductivity in stratified NaCl solutions.
[electronic resource]
by
Sheppard, D M
Doddington, H W
Producer:
19770718
In:
The Review of scientific instruments
vol. 48
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4.
Karyotypic analysis of the human monoblastic cell line U937.
[electronic resource]
by
Shipley, J M
Sheppard, D M
Sheer, D
Producer:
19880330
In:
Cancer genetics and cytogenetics
vol. 30
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5.
Translocation 1;7 in four cases of myeloid disorders.
[electronic resource]
by
Sheppard, D M
Richkind, K E
Bull, M
Producer:
19890615
In:
Cancer genetics and cytogenetics
vol. 38
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6.
Purification of uroporphyrinogen decarboxylase from human erythrocytes. Immunochemical evidence for a single protein with decarboxylase activity in human erythrocytes and liver.
[electronic resource]
by
Elder, G H
Tovey, J A
Sheppard, D M
Producer:
19831123
In:
The Biochemical journal
vol. 215
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7.
Twin pregnancy with complete hydatidiform mole (46,XX) and fetus (46,XY): genetic origin proved by analysis of chromosome polymorphisms.
[electronic resource]
by
Fisher, R A
Sheppard, D M
Lawler, S D
Producer:
19820722
In:
British medical journal (Clinical research ed.)
vol. 284
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8.
Studies on human phenylalanine Mono-oxygenase. I. Restricted expression.
[electronic resource]
by
Crawfurd, M D
Gibbs, D A
Sheppard, D M
Producer:
19820222
In:
Journal of inherited metabolic disease
vol. 4
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9.
Two patients with complete hydatidiform mole with 46,XY karyotype.
[electronic resource]
by
Fisher, R A
Sheppard, D M
Lawler, S D
Producer:
19840829
In:
British journal of obstetrics and gynaecology
vol. 91
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10.
Abnormal line bisection judgements in children with Tourette's syndrome.
[electronic resource]
by
Sheppard, D M
Bradshaw, J L
Mattingley, J B
Producer:
20020320
In:
Neuropsychologia
vol. 40
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11.
Karyotypic analysis and chromosome polymorphisms in four choriocarcinoma cell lines.
[electronic resource]
by
Sheppard, D M
Fisher, R A
Lawler, S D
Producer:
19850430
In:
Cancer genetics and cytogenetics
vol. 16
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12.
Tourette's and comorbid syndromes: obsessive compulsive and attention deficit hyperactivity disorder. A common etiology?
[electronic resource]
by
Sheppard, D M
Bradshaw, J L
Purcell, R
Pantelis, C
Producer:
19991014
In:
Clinical psychology review
vol. 19
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13.
Tetraploid conceptus with three paternal contributions.
[electronic resource]
by
Sheppard, D M
Fisher, R A
Lawler, S D
Povey, S
Producer:
19830527
In:
Human genetics
vol. 62
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14.
Effects of stimulant medication on the lateralisation of line bisection judgements of children with attention deficit hyperactivity disorder.
[electronic resource]
by
Sheppard, D M
Bradshaw, J L
Mattingley, J B
Lee, P
Producer:
19990204
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 66
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15.
Building a novel occupational rehabilitation program to support cancer survivors to return to health, wellness, and work in Australia.
[electronic resource]
by
Sheppard, D M
Frost, D
Jefford, M
O'Connor, M
Halkett, G
Producer:
20200923
In:
Journal of cancer survivorship : research and practice
vol. 14
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16.
Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase.
[electronic resource]
by
Elder, G H
Sheppard, D M
De Salamanca, R E
Olmos, A
Producer:
19810116
In:
Clinical science (London, England : 1979)
vol. 58
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17.
Immunoreactive uroporphyrinogen decarboxylase in porphyria cutanea tarda.
[electronic resource]
by
Elder, G H
Sheppard, D M
Tovey, J A
Urquhart, A J
Producer:
19830715
In:
Lancet (London, England)
vol. 1
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18.
Movement sequencing in children with Tourette's syndrome and attention deficit hyperactivity disorder.
[electronic resource]
by
Sheppard, D M
Bradshaw, J L
Georgiou, N
Bradshaw, J A
Lee, P
Producer:
20010531
In:
Movement disorders : official journal of the Movement Disorder Society
vol. 15
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19.
Cytogenetic analysis of four human ovarian carcinoma cell lines.
[electronic resource]
by
Sheer, D
Sheppard, D M
Gorman, P A
Ward, B
Whelan, R D
Hill, B T
Producer:
19870619
In:
Cancer genetics and cytogenetics
vol. 26
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20.
Localization of the oncogene c-erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17.
[electronic resource]
by
Sheer, D
Sheppard, D M
le Beau, M
Rowley, J D
San Roman, C
Solomon, E
Producer:
19860109
In:
Annals of human genetics
vol. 49
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