Associated Papers
Effect of clinical whole exome sequencing in aetiological investigation and reproductive risk prediction for a couple with monogenic inherited diseases.
Wang Y et al.
Frontiers in Genetics, 2024
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.
Zin OA et al.
Genes, 2021
34356085 (PubMed )
Supplement: genes-12-01069-s001.zip › genes-1253197-supplementary.pdf
Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.
Ma AS et al.
Human Mutation, 2016
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