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Results of search for 'au:"Kaiser-Rogers, K"'
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Authors
Aylsworth, A S
Calikoglu, A S
Dansereau, J
Elder, D A
Funkhouser, W K
Gu, J J
Jiang, R
Kaiser-Rogers, K
Kaiser-Rogers, K A
Knops, J F
Lefebvre, L
Lese, C M
Livasy, C A
Matson, S W
McFadden, D E
Mendonca, V M
Michaelis, R C
Mitchell, B S
Powell, C M
Rao, K W
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Topics
Abnormalities, Multiple
Adenosine Triphosphatases
Adult
Androgens
Animals
Antigens, Viral, Tumor
Base Sequence
Child
DNA Helicases
Escherichia coli
Female
Humans
In Situ Hybridization, Fluorescence
Karyotyping
Male
Molecular Sequence Data
Phenotype
Syndrome
genetics
metabolism
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English
Your search returned 7 results.
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1.
Review: significance of, and optimal screening for, HER-2 gene amplification and protein overexpression in breast carcinoma.
[electronic resource]
by
Funkhouser, W K
Kaiser-Rogers, K
Producer:
20020322
In:
Annals of clinical and laboratory science
vol. 31
Availability:
No items available.
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2.
DNA helicases.
[electronic resource]
by
Matson, S W
Kaiser-Rogers, K A
Producer:
19900830
In:
Annual review of biochemistry
vol. 59
Online resources:
Available from publisher's website
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3.
Double helicase II (uvrD)-helicase IV (helD) deletion mutants are defective in the recombination pathways of Escherichia coli.
[electronic resource]
by
Mendonca, V M
Kaiser-Rogers, K
Matson, S W
Producer:
19930825
In:
Journal of bacteriology
vol. 175
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4.
Assignment of the human type I IMP dehydrogenase gene (IMPDH1) to chromosome 7q31.3-q32).
[electronic resource]
by
Gu, J J
Kaiser-Rogers, K
Rao, K
Mitchell, B S
Producer:
19950421
In:
Genomics
vol. 24
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5.
Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome.
[electronic resource]
by
Elder, D A
Kaiser-Rogers, K
Aylsworth, A S
Calikoglu, A S
Producer:
20010712
In:
American journal of medical genetics
vol. 101
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6.
Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements.
[electronic resource]
by
Kaiser-Rogers, K A
Rao, K W
Michaelis, R C
Lese, C M
Powell, C M
Producer:
20001130
In:
American journal of medical genetics
vol. 95
Online resources:
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7.
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia.
[electronic resource]
by
Kaiser-Rogers, K A
McFadden, D E
Livasy, C A
Dansereau, J
Jiang, R
Knops, J F
Lefebvre, L
Rao, K W
Robinson, W P
Producer:
20060811
In:
Journal of medical genetics
vol. 43
Online resources:
Available from publisher's website
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