Alerts
PDF
Other content recommended for you
- Somatic mosaicism containing double mutations in PTCH1 revealed by generation of induced pluripotent stem cells from nevoid basal cell carcinoma syndrome
- Parkes-Weber syndrome in the emergency department
- Sturge-Weber syndrome type III: an important stroke mimic
- Dermatological clues to neurological diagnoses
- Life expectancy in hereditary cancer predisposing diseases: an observational study
- Neurocutaneous disorders
- Diagnosis of sporadic neurofibromatosis type 2 in the paediatric population
- Mosaicism in sporadic neurofibromatosis type 1: variations on a theme common to other hereditary cancer syndromes?
- Sturge-Weber syndrome type 3 manifesting as ‘Status migrainosus’
- Encephalocraniocutaneous lipomatosis phenotype associated with mosaic biallelic pathogenic variants in the NF1 gene