advertisement

Topcon

Cai S 13

Showing records 1 to 13 | Display all abstracts from Cai S

95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Cai S
Molecular medicine reports 2021; 24:
96279 Metabolomics in Retinal Diseases: An Update
Li X
Biology 2021; 10:
95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Zhang D
Molecular medicine reports 2021; 24:
96279 Metabolomics in Retinal Diseases: An Update
Cai S
Biology 2021; 10:
95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Jiao X
Molecular medicine reports 2021; 24:
96279 Metabolomics in Retinal Diseases: An Update
He Z; Reilly J
Biology 2021; 10:
95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Wang T
Molecular medicine reports 2021; 24:
96279 Metabolomics in Retinal Diseases: An Update
Zeng Z
Biology 2021; 10:
95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Fan M
Molecular medicine reports 2021; 24:
96279 Metabolomics in Retinal Diseases: An Update
Strang N
Biology 2021; 10:
95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Wang Y; Hejtmancik JF
Molecular medicine reports 2021; 24:
96279 Metabolomics in Retinal Diseases: An Update
Shu X
Biology 2021; 10:
95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Liu X
Molecular medicine reports 2021; 24:

Issue 22-3

Change Issue


advertisement

Nidek