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Results of search for 'au:"Killeen, A A"', page 1 of 2
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Authors
Akel, N
Askari, F K
Bavikatty, N R
Bowers, L D
Cairl, C J
Chai, C
Crotty, P L
Dean, J J
Filipovich, A H
Jiddou, R R
Killeen, A A
Lubman, D M
Orr, H T
Ozturk, I C
Ramey, M L
Sane, K S
Siemieniak, D
Srinivasan, J R
Wei, W L
Yasmineh, W G
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Topics
Adolescent
Adrenal Hyperplasia, Congenital
Adult
Alleles
Base Sequence
Bone Marrow Transplantation
Child
DNA
Female
Humans
Male
Molecular Sequence Data
Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Steroid 21-Hydroxylase
analysis
blood
genetics
methods
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English
Your search returned 30 results.
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1.
Overview of current Internet resources for molecular pathology.
[electronic resource]
by
Killeen, A A
Producer:
19970307
In:
Journal of clinical laboratory analysis
vol. 10
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2.
Molecular genetic pathology: an exam, finally.
[electronic resource]
by
Killeen, A A
Producer:
20020318
In:
Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology
vol. 6
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3.
Quantification of nucleic acids.
[electronic resource]
by
Killeen, A A
Producer:
19970502
In:
Clinics in laboratory medicine
vol. 17
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4.
Commentary: molecular analysis of congenital adrenal hyperplasia in a newborn screening program.
[electronic resource]
by
Killeen, A A
Producer:
20011205
In:
Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology
vol. 6
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5.
Carbamazepine measurement in samples from the emergency room.
[electronic resource]
by
Chai, C
Killeen, A A
Producer:
19941228
In:
Therapeutic drug monitoring
vol. 16
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6.
An overview of molecular diagnosis of steroid 21-hydroxylase deficiency.
[electronic resource]
by
Keegan, C E
Killeen, A A
Producer:
20010719
In:
The Journal of molecular diagnostics : JMD
vol. 3
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7.
BRCA1 mutation testing: controversies and challenges.
[electronic resource]
by
Petty, E M
Killeen, A A
Producer:
19970130
In:
Clinical chemistry
vol. 43
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8.
Fetal supraventricular tachycardia treated with high-dose quinidine: toxicity associated with marked elevation of the metabolite, 3(S)-3-hydroxyquinidine.
[electronic resource]
by
Killeen, A A
Bowers, L D
Producer:
19870925
In:
Obstetrics and gynecology
vol. 70
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9.
An overview of genetic factors influencing plasma lipid levels and coronary artery disease risk.
[electronic resource]
by
Ozturk, I C
Killeen, A A
Producer:
20000106
In:
Archives of pathology & laboratory medicine
vol. 123
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10.
Catalase, superoxide dismutase and glutathione peroxidase activity in neutrophils of sham-operated and olfactory-bulbectomised rats following chronic treatment with desipramine and lithium chloride.
[electronic resource]
by
Song, C
Killeen, A A
Leonard, B E
Producer:
19941220
In:
Neuropsychobiology
vol. 30
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11.
Evaluation of chimerism in DNA samples by PCR amplification of D1S80 with detection by capillary electrophoresis.
[electronic resource]
by
Jone, C M
Akel, N
Killeen, A A
Producer:
20001121
In:
Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology
vol. 5
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12.
Genotyping of apolipoprotein e.
[electronic resource]
by
Ozturk, I C
Akel, N
Killeen, A A
Producer:
20121002
In:
Methods in molecular medicine
vol. 49
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13.
Molecular and endocrine characterization of a mutation involving a recombination between the steroid 21-hydroxylase functional gene and pseudogene.
[electronic resource]
by
Killeen, A A
Sane, K S
Orr, H T
Producer:
19910813
In:
The Journal of steroid biochemistry and molecular biology
vol. 38
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14.
Conjugated hyperbilirubinemia and renal function in bone marrow transplant recipients.
[electronic resource]
by
Yasmineh, W G
Killeen, A A
Filipovich, A H
Producer:
19880328
In:
Archives of pathology & laboratory medicine
vol. 112
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15.
Chromosomal aneuploidy in leukemic blast crisis: a potential source of error in interpretation of bone marrow engraftment analysis by VNTR amplification.
[electronic resource]
by
Zhou, M
Sheldon, S
Akel, N
Killeen, A A
Producer:
19990914
In:
Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology
vol. 4
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16.
Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles.
[electronic resource]
by
Killeen, A A
Jiddou, R R
Sane, K S
Producer:
19990105
In:
Clinical chemistry
vol. 44
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17.
Serum 5'nucleotidase and alkaline phosphatase--highly predictive liver function tests for the diagnosis of graft-versus-host disease in bone marrow transplant recipients.
[electronic resource]
by
Yasmineh, W G
Filipovich, A H
Killeen, A A
Producer:
19891219
In:
Transplantation
vol. 48
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18.
High-dose hook effect in an immunoluminometric thyrotropin assay: the open-faced sandwich artefact.
[electronic resource]
by
Killeen, A A
Ramey, M L
Dean, J J
Producer:
19931020
In:
Annals of clinical biochemistry
vol. 30 ( Pt 4)
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19.
Diagnosis of classical steroid 21-hydroxylase deficiency using an HLA-B locus-specific DNA-probe.
[electronic resource]
by
Killeen, A A
Seelig, S
Ulstrom, R A
Orr, H T
Producer:
19880624
In:
American journal of medical genetics
vol. 29
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20.
Sequence analysis of the hepatitis C virus (HCV) core gene suggests the core protein as an appropriate target for HCV vaccine strategies.
[electronic resource]
by
Hitomi, Y
McDonnell, W M
Killeen, A A
Askari, F K
Producer:
19961206
In:
Journal of viral hepatitis
vol. 2
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