Your selections:
FOXP1 mutations cause intellectual disability and a recognizable phenotype
- Le Fevre, Anna K., Taylor, Sharelle, Bain, Nicole, Fagan, Kerry, Hunter, Matthew F., Malek, Neva H., Horn, Denise, Carr, Christopher W., Abdul-Rahman, Omar A., O'Donnell, Sherindan, Burgess, Trent, Shaw, Marie, Gecz, Jozef
Elevated serum tissue transglutaminase antibodies in children with eosinophilic esophagitis
- Le Fevre, Anna K., Walker, Marjorie M., Hadjiashrafy, Amir, Bhatia, Rani, Mattes, Joerg, Talley, Nicholas J., Nightingale, Scott
Are you sure you would like to clear your session, including search history and login status?