Associated Papers
A novel de novo TP63 mutation in whole-exome sequencing of a Syrian family with Oral cleft and ectrodactyly.
Simpson CL et al.
Molecular Genetics & Genomic Medicine, 2023
37070724 (PubMed )
Supplement: MGG3-11-e2179-s002.xlsx › Supplementary_Table_S2
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease.
Moll M et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology, 2021
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