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/vufind/Search/Results?lookfor=%22Ko%2C+Jung+Min%22&type=Person&sort=year
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PubPharm (227)
1
Development of disease-specific growth charts for Korean children with Beckwith-Wiedemann syndrome
enthalten in:
Clinical genetics
| 2024
von
Choi, N.
|
Kim, H.
|
Ko, J.
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2
Familial chylomicronemia syndrome : case reports of siblings with deletions of the GPIHBP1 gene
enthalten in:
BMC endocrine disorders
| 2024
von
Kim, K.
|
Heo, Y.
|
Ko, J.
| +4
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3
Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene
enthalten in:
BMC endocrine disorders
| 2024
von
Kim, K.
|
Heo, Y.
|
Ko, J.
| +4
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4
Clinical practices and prognosis of Congenital Central Hypoventilation Syndrome : based on 20-year-records in Korea
enthalten in:
ResearchSquare.com
| 2024
von
Lee, M.
|
Park, J.
|
Kim, K.
| +3
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5
De novo HDAC3
variants leading to epigenetic machinery dysfunction are associated with a neurodevelopmental disorder
enthalten in:
bioRxiv.org
| 2024
von
Yoon, J.
|
Lim, S.
|
Seo, H.
| +9
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6
Development of disease‐specific growth charts for Korean children with Beckwith–Wiedemann syndrome
enthalten in:
Clinical Genetics
| 2024
von
Choi, N.
|
Kim, H.
|
Ko, J.
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7
Systematic analysis of Mendelian disease-associated gene variants reveals new classes of cancer-predisposing genes
enthalten in:
Genome medicine
| 2023
von
Song, S.
|
Koh, Y.
|
Kim, S.
| +6
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8
Systematic analysis of Mendelian disease-associated gene variants reveals new classes of cancer-predisposing genes
enthalten in:
Genome medicine
| 2023
von
Song, S.
|
Koh, Y.
|
Kim, S.
| +6
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9
Recurrent Vascularizing Keratitis in Infants With Hereditary Mucoepithelial Dysplasia Related to SREBF1 Mutation
enthalten in:
Cornea
| 2023
von
Kim, S.
|
Jeong, H.
|
Ko, J.
| +2
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10
Cardiovascular Characteristics and Progressions of Hypertrophic Cardiomyopathy and Pulmonary Stenosis in RASopathy Syndrome in the Genomic Era
enthalten in:
The Journal of pediatrics
| 2023
von
Kim, S.
|
Lee, S.
|
Kim, G.
| +3
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Orphanet journal of rare diseases
16
European journal of pediatrics
13
Journal of human genetics
10
Annals of clinical and laboratory science
9
Journal of Korean medical science
8
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6
BMC medical genetics
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Endocrine journal
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ResearchSquare.com
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European journal of medical genetics
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bioRxiv.org
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Annals of dermatology
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Annals of pediatric endocrinology & metabolism
4
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3
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3
Clinics in orthopedic surgery
3
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570
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Achondroplasia
6
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6
Letter
5
Nuclear Proteins
5
Rare disease
5
Undiagnosed disease program
4
12629-01-5
4
Antley-Bixler syndrome
4
Bartter syndrome
4
Bartter-like phenotype
4
Beckwith–Wiedemann syndrome
4
Craniosynostosis
4
Failure to thrive
4
Foramen magnum decompression
4
Human Growth Hormone
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