Search

Search Constraints

You searched for: Author/Creator Wei, Heming

Search Results

1. A novel NSDHL variant in CHILD syndrome with gastrointestinal manifestations and localized skin involvement. Issue 1 (26th December 2021)

6. Clinical features of a male with a USP9X variant associated with intellectual disability: A case study and review of reported cases. Issue 2 (4th November 2021)

8. Corrigendum to Cardiomyocyte differentiation of pluripotent stem cells with SB203580 analogues correlates with Wnt pathway CK1 inhibition independent of p38 MAPK signaling [J Mol Cell Cardiol 80 (2015) 56–70]. (August 2015)