Suchergebnisse - "Seong, Moon-Woo"

PubPharm (8)

1

Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients

enthalten in: Journal of glaucoma | 2020

von Kim, M. | Kim, Y. | Jeoung, J. | +8

2

Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient

enthalten in: Korean journal of ophthalmology : KJO | 2020

von Lee, Y. | Joo, K. | Seong, M. | +3

3

Retinitis Pigmentosa Associated with Bardet-Biedl Syndrome with BBS9 Gene Mutation in a Korean Patient

enthalten in: Korean journal of ophthalmology : KJO | 2020

von Kim, Y. | Joo, K. | Seong, M. | +2

4

Large Deletions of TSPAN12 Cause Familial Exudative Vitreoretinopathy (FEVR)

enthalten in: Investigative ophthalmology & visual science | 2016

von Seo, S. | Kim, M. | Park, S. | +11

5

Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy

enthalten in: Investigative ophthalmology & visual science | 2015

von Seo, S. | Yu, Y. | Park, S. | +8

6

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

7

Non-homologous end joining repair mechanism-mediated deletion of CHD7 gene in a patient with typical CHARGE syndrome

enthalten in: Annals of laboratory medicine | 2015

von Lee, S. | Chae, J. | Lee, J. | +5

8

Molecular identification of the novel Gγ-β hybrid hemoglobin : Hb Gγ-β Ulsan (Gγ through 13; β from 19)

enthalten in: Blood cells, molecules & diseases | 2010

von Kim, S. | Lee, S. | Cho, S. | +12

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