Associated Papers
Unexpected High Prevalence of Focal Facial Dermal Dysplasia (FFDD) Type IV Is Linked to a Founder Effect in the Belgian Population.
Beyens A et al.
Clinical Genetics, 2025
Whole genome sequencing unveils genetic heterogeneity in optic nerve hypoplasia.
Dahl S et al.
Plos One, 2020
Focal facial dermal dysplasia type 4: identification of novel CYP26C1 mutations in unrelated patients.
Lee BH et al.
Journal of Human Genetics, 2018
NCI-60 whole exome sequencing and pharmacological CellMiner analyses.
Reinhold WC et al.
Plos One, 2014
25032700 (PubMed )
Supplement: pone.0101670.s001.xlsx › Supplementary_Table_1
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