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Results of search for 'au:"Ki, C-S"', page 1 of 2
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Authors
Cho, D
Cho, E-H
Cho, H-J
Cho, S Y
Choi, E W
Huh, H J
Jin, D-K
Ki, C S
Ki, C-S
Kim, H J
Kim, H-J
Kim, J W
Kim, J-W
Kim, S J
Lee, N Y
Lee, S-T
Lee, S-Y
Lee, Y-W
Na, D L
Park, H-D
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Adolescent
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Age of Onset
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Asian People
Base Sequence
Child
Child, Preschool
DNA Mutational Analysis
Female
Gene Frequency
Genotype
Humans
Korea
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diagnosis
genetics
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English
Your search returned 36 results.
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1.
Molecular characterization of enteroviruses isolated from patients with aseptic meningitis in Korea, 2005.
[electronic resource]
by
Lee, S-T
Ki, C-S
Lee, N Y
Producer:
20070914
In:
Archives of virology
vol. 152
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2.
Mutation analysis of the genes involved in the Ras-mitogen-activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome.
[electronic resource]
by
Lee, S-T
Ki, C-S
Lee, H J
Producer:
20071105
In:
Clinical genetics
vol. 72
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3.
Frequencies of 10 autosomal minor histocompatibility antigens in Korean population and estimated disparities in unrelated hematopoietic stem cell transplantation.
[electronic resource]
by
Jung, H
Ki, C S
Kim, J W
Kang, E S
Producer:
20120416
In:
Tissue antigens
vol. 79
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4.
Mitochondrial GTPase mitofusin 2 mutations in Korean patients with Charcot-Marie-Tooth neuropathy type 2.
[electronic resource]
by
Cho, H-J
Sung, D H
Kim, B J
Ki, C-S
Producer:
20070614
In:
Clinical genetics
vol. 71
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5.
Radiological Findings of Two Sisters with Aceruloplasminemia Presenting with Chorea.
[electronic resource]
by
Kim, H K
Ki, C S
Kim, Y J
Lee, M S
Producer:
20181121
In:
Clinical neuroradiology
vol. 27
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6.
Alpha-1 antichymotrypsin and alpha-2 macroglobulin gene polymorphisms are not associated with Korean late-onset Alzheimer's disease.
[electronic resource]
by
Ki, C S
Na, D L
Kim, H J
Kim, J W
Producer:
20010712
In:
Neuroscience letters
vol. 302
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7.
Carrier frequency of the R778L, A874V, and N1270S mutations in the ATP7B gene in a Korean population.
[electronic resource]
by
Park, H-D
Ki, C-S
Lee, S-Y
Kim, J-W
Producer:
20090722
In:
Clinical genetics
vol. 75
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8.
Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1.
[electronic resource]
by
Park, H-K
Kim, B J
Sung, D H
Ki, C-S
Kim, J-W
Producer:
20061108
In:
Clinical genetics
vol. 70
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9.
Late-onset vanishing white matter disease with compound heterozygous EIF2B5 gene mutations.
[electronic resource]
by
Lee, H-N
Koh, S-H
Lee, K-Y
Ki, C-S
Lee, Y J
Producer:
20090709
In:
European journal of neurology
vol. 16
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10.
Lack of association of the interleukin-1alpha gene polymorphism with Alzheimer's disease in a Korean population.
[electronic resource]
by
Ki, C S
Na, D L
Kim, D K
Kim, H J
Kim, J W
Producer:
20010628
In:
Annals of neurology
vol. 49
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11.
Effects of warm acupuncture on breast cancer-related chronic lymphedema: a randomized controlled trial.
[electronic resource]
by
Yao, C
Xu, Y
Chen, L
Jiang, H
Ki, C S
Byun, J S
Bian, W
Producer:
20160311
In:
Current oncology (Toronto, Ont.)
vol. 23
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12.
Frequency of FMR1 premutation carriers and rate of expansion to full mutation in a retrospective diagnostic FMR1 Korean sample.
[electronic resource]
by
Jang, J-H
Lee, K
Cho, E-H
Lee, E-H
Kim, J-W
Ki, C-S
Producer:
20141121
In:
Clinical genetics
vol. 85
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13.
Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation.
[electronic resource]
by
Yoon, W T
Lee, W Y
Lee, S-T
Ahn, J Y
Ki, C-S
Cho, J W
Producer:
20120406
In:
European journal of neurology
vol. 19
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14.
Frequency of DMPK mutation carriers in Korean women of childbearing age.
[electronic resource]
by
Jang, J-H
Lee, J W
Cho, E-H
Lee, E-H
Kim, J-W
Ki, C-S
Producer:
20150525
In:
Clinical genetics
vol. 86
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15.
Epstein-Barr virus reactivation in extranodal natural killer/T-cell lymphoma patients: a previously unrecognized serious adverse event in a pilot study with romidepsin.
[electronic resource]
by
Kim, S J
Kim, J H
Ki, C S
Ko, Y H
Kim, J S
Kim, W S
Producer:
20161213
In:
Annals of oncology : official journal of the European Society for Medical Oncology
vol. 27
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16.
Silent infarcts demonstrated by diffusion-weighted MRI in CADASIL.
[electronic resource]
by
Moon, S Y
Ki, C S
Kim, J W
Suh, Y L
Kwon, J C
Na, D L
Producer:
20030429
In:
European neurology
vol. 49
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17.
No association between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer's disease.
[electronic resource]
by
Ki, C S
Na, D L
Kim, J W
Kim, H J
Kim, D K
Yoon, B K
Producer:
19990628
In:
American journal of medical genetics
vol. 88
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18.
The Ala53Thr mutation in the alpha-synuclein gene in a Korean family with Parkinson disease.
[electronic resource]
by
Ki, C-S
Stavrou, E F
Davanos, N
Lee, W Y
Chung, E J
Kim, J-Y
Athanassiadou, A
Producer:
20070725
In:
Clinical genetics
vol. 71
Online resources:
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19.
Direct application of the PCR restriction analysis method for identifying NTM species in AFB smear-positive respiratory specimens.
[electronic resource]
by
Kim, S
Park, E M
Kwon, O J
Lee, J H
Ki, C-S
Lee, N Y
Koh, W-J
Producer:
20090204
In:
The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease
vol. 12
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20.
Clinical and genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome.
[electronic resource]
by
Lee, Y-W
Kim, S C
Shin, Y L
Kim, J-W
Hong, H S
Lee, Y K
Ki, C-S
Producer:
20090408
In:
Clinical genetics
vol. 75
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