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Keyword [SNRNP200]
Result: 1 - 3 | Page: 1 of 1
1.
A Novel Missense SNRNP200Mutation Associated With Autosomal Dominant Retinitis Pigmentosa In A Chinese Family
2.
Molecular Genetics Analysis And Pathogenesis Study Of Hereditary Retinal Diseases
3.
Genetic Screening Of An RP Family And The Study Of IPS-RPE Cells Of Patients
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