Associated Papers
Subtle phenotypes of Mowat-Wilson syndrome in a patient with a novel ZEB2 C-ZF domain variant.
Kuroda Y et al.
American Journal of Medical Genetics. Part A, 2024
Letter regarding the article "Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals ()" and the diagnosis of coexisting Mowat-Wilson syndrome in a patient with 16p11.2 deletion.
Amor DJ et al.
European Journal of Medical Genetics, 2018
Select a paper to view details