Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Jingjun Xiao"'
Autor:
Sifeng Wang, Shuyuan Yan, Jingjun Xiao, Ying Chen, Anji Chen, Aimin Deng, Tuanmei Wang, Jun He, Xiangwen Peng
Publikováno v:
Molecular Cytogenetics, Vol 16, Iss 1, Pp 1-5 (2023)
Abstract Background Wiedemann–Steiner syndrome (WDSTS) is a rare autosomal dominant disorder caused by mutations in the KMT2A gene and is usually characterized by hairy elbows, short stature, developmental delay, intellectual disability and obvious
Externí odkaz:
https://doaj.org/article/e4b80ad42b944357a225e0a8f39809fc
