Associated Papers
STARD9 and CDK5RAP2-Novel Candidate Genes for 46,XY Complete Gonadal Dysgenesis.
Sirokha D et al.
International Journal of Molecular Sciences, 2025
Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations.
Bujakowska KM et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
Integrated genomic analyses of de novo pathways underlying atypical meningiomas.
Harmancı AS et al.
Nature Communications, 2017
28195122 (PubMed )
Supplement: ncomms14433-s3.xlsx › Table_S2D
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