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/vufind/Search/Results?lookfor=%22Lin%2C+Qinghong%22&type=Person&sort=year
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PubPharm (32)
1
Genetic investigation in a four-generation Chinese family with congenital fibrosis of extraocular muscles and keratoconus
enthalten in:
Heliyon
| 2024
von
Lin, Q.
|
Wang, X.
|
Zhan, X.
| +3
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2
Variants in the ZNF469 gene in families with Brittle cornea syndrome and keratoconus
enthalten in:
Heliyon
| 2024
von
Lin, Q.
|
Wang, X.
|
Han, T.
| +2
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3
Identification of genetic variants in two families with Keratoconus
enthalten in:
BMC medical genomics
| 2023
von
Lin, Q.
|
Wang, X.
|
Han, T.
| +1
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4
Identification of genetic variants in two families with Keratoconus
enthalten in:
BMC medical genomics
| 2023
von
Lin, Q.
|
Wang, X.
|
Han, T.
| +1
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5
Intensive topical steroid regimen for enhanced very early recovery after small incision lenticule extraction
enthalten in:
International ophthalmology
| 2023
von
Lin, Q.
|
Shen, Z.
|
Zhou, X.
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6
LncRNA-XR_002792574.1-mediated ceRNA network reveals potential biomarkers in myopia-induced retinal ganglion cell damage
enthalten in:
Journal of translational medicine
| 2023
von
Wang, X.
|
Lin, Q.
|
Liu, S.
| +9
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7
LncRNA-XR_002792574.1-mediated ceRNA network reveals potential biomarkers in myopia-induced retinal ganglion cell damage
enthalten in:
Journal of translational medicine
| 2023
von
Wang, X.
|
Lin, Q.
|
Liu, S.
| +9
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8
The role of mip in the development of lens in zebrafish
enthalten in:
Gene expression patterns : GEP
| 2023
von
He, M.
|
Zhou, G.
|
Lin, Q.
| +1
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9
Flexible Quantum Dot Light-Emitting Device for Emerging Multifunctional and Smart Applications
enthalten in:
Advanced materials (Deerfield Beach, Fla.)
| 2023
von
Lin, Q.
|
Zhu, Y.
|
Wang, Y.
| +5
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10
New splice site mutations in MYO7A causing Usher syndrome type 1 : a study on a Chinese consanguineous family
enthalten in:
International ophthalmology
| 2023
von
Lin, Q.
|
Yang, D.
|
Shen, Z.
| +1
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