P63 gene mutations and human developmental syndromes
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference38 articles.
1. TP63 gene mutation in ADULT syndrome
2. Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes
3. Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome
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3. The Splicing Factor PTBP1 Represses TP63 γ Isoform Production in Squamous Cell Carcinoma;Cancer Research Communications;2022-12-20
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