Disease: Kaplowitz Bodurtha syndrome
- A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency
- Glucose to Lymphocyte Ratio as a Prognostic Marker in Patients With Resected pT2 Gallbladder Cancer
- Midterm results of anatomic repair in a subgroup of corrected transposition
- Monozygotic twins discordant for Ullrich-Turner syndrome
- The phenotypic spectrum associated with OTX2 mutations in humans