Associated Papers
Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants.
Hurni Y et al.
Clinical Case Reports, 2021
TP63-truncating variants cause isolated premature ovarian insufficiency.
Tucker EJ et al.
Human Mutation, 2019
Genetic analysis of a congenital split‑hand/split‑foot malformation 4 pedigree.
Yang X et al.
Molecular Medicine Reports, 2018
P63 mutations are not a major cause of non-syndromic split hand/foot malformation.
de Mollerat XJ et al.
Journal of Medical Genetics, 2003
Select a paper to view details