Associated Papers
A Novel Homozygous Synonymous Variant in CCDC134 as a Cause of Osteogenesis Imperfecta Type XXII.
Ning H et al.
Clinical Genetics, 2025
Identification of Novel Candidate Genes for Familial Thyroid Cancer by Whole Exome Sequencing.
Tous C et al.
International Journal of Molecular Sciences, 2023
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