Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformations
Ryan P. Liegel(Cincinnati Children's Hospital Medical Center), Rolf W. Stottmann(Nationwide Children's Hospital)
Cited by 5
Related Papers
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
|The American Journal of Human Genetics|2019|85
A mutational hotspot in <scp><i>AMOTL1</i></scp> defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature
|American Journal of Medical Genetics Part A|2023|3
Dkk1 inhibition normalizes limb phenotypes in a mouse model of <i>Fzd2</i> associated omodysplasia Robinow syndromes
|bioRxiv (Cold Spring Harbor Laboratory)|2022|0