Associated Papers
Novel de novo mutation in ZBTB20 in a Chinese Primrose syndrome family and a review of the literature.
Li J et al.
Molecular Genetics & Genomic Medicine, 2024
Unique skeletal manifestations in patients with Primrose syndrome.
Arora V et al.
European Journal of Medical Genetics, 2020
Primrose syndrome: Characterization of the phenotype in 42 patients.
Melis D et al.
Clinical Genetics, 2020
Select a paper to view details