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/vufind/Search/Results?filter%5B%5D=topic_facet%3A%22Journal+Article%22&filter%5B%5D=topic_facet%3A%22Case+Reports%22&lookfor=%22Seong%2C+Moon-Woo%22&type=Person
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PubPharm (26)
1
Cryptic KMT2A/MLLT10 fusion detected by next-generation sequencing in a case of pediatric acute megakaryoblastic leukemia
enthalten in:
Cancer genetics
| 2023
von
Kim, Y.
|
Kim, B.
|
Seong, M.
| +5
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2
A Novel Missense PRKAR1A Variant Causes Carney Complex
enthalten in:
Endocrinology and metabolism (Seoul, Korea)
| 2022
von
Kim, B.
|
Jang, H.
|
Chae, K.
| +5
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3
Novel HEXA variants in Korean children with Tay-Sachs disease with regression of neurodevelopment from infancy
enthalten in:
Molecular genetics & genomic medicine
| 2021
von
Park, J.
|
Ko, J.
|
Kim, M.
| +5
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4
Sequential Analysis of Viral Load in a Neonate and Her Mother Infected With Severe Acute Respiratory Syndrome Coronavirus 2
enthalten in:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
| 2020
von
Han, M.
|
Seong, M.
|
Heo, E.
| +6
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5
A cluster of tertiary transmissions of 2019 novel coronavirus (SARS-CoV-2) in the community from infectors with common cold symptoms
enthalten in:
The Korean journal of internal medicine
| 2020
von
Kim, N.
|
Choe, P.
|
Park, S.
| +6
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6
Virus Isolation from the First Patient with SARS-CoV-2 in Korea
enthalten in:
Journal of Korean medical science
| 2020
von
Park, W.
|
Kwon, N.
|
Choi, S.
| +9
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7
Pediatric Case Report on an Interstitial Lung Disease with a Novel Mutation of SFTPC Successfully Treated with Lung Transplantation
enthalten in:
Journal of Korean medical science
| 2018
von
Park, J.
|
Choi, Y.
|
Kim, Y.
| +10
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8
COQ6 Mutations in Children With Steroid-Resistant Focal Segmental Glomerulosclerosis and Sensorineural Hearing Loss
enthalten in:
American journal of kidney diseases : the official journal of the National Kidney Foundation
| 2017
von
Park, E.
|
Ahn, Y.
|
Kang, H.
| +8
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9
Clinical and Molecular Delineation of a Novel Cys1050Phe Missense Mutation in the ABCC9 Gene in a Korean Patient with Cantú Syndrome
enthalten in:
Clinical laboratory
| 2017
von
Kim, H.
|
Kim, S.
|
Jeon, H.
| +4
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10
Biochemical and Genetic Analysis of Seven Korean Individuals With Suspected Metachromatic Leukodystrophy
enthalten in:
Annals of laboratory medicine
| 2015
von
Han, M.
|
Jun, S.
|
Lee, Y.
| +7
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