Prenatally Diagnosed Beare‐Stevenson Cutis Gyrata Syndrome With a Novel FGFR2 Variant
Abstract
Key Points What is already known about this topic? What does this study add?
Fields of Study & Subjects
Genetic and rare skin diseases.
Genomics and Rare Diseases
Connective tissue disorders research
Publication details
- Journal / source
- Prenatal Diagnosis
- Volume
- 46
- Issue
- 4
- Pages
- 589–592
- Publication date
- 3 March 2026
- Language
- EN