Search

Search Constraints

You searched for: Author/Creator Hogan, Benjamin M.

Search Results

1. Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. Issue 1 (21st October 2019)

2. Carbamoyl‐phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase (cad) regulates Notch signaling and vascular development in zebrafish. Issue 1 (17th November 2014)

4. Expanding the genotypic spectrum of CCBE1 mutations in Hennekam syndrome. Issue 10 (27th June 2016)

5. In vivo mutation of pre‐mRNA processing factor 8 (Prpf8) affects transcript splicing, cell survival and myeloid differentiation. Issue 14 (25th May 2013)

10. Pkd1 and Wnt5a genetically interact to control lymphatic vascular morphogenesis in mice. Issue 2 (16th July 2021)