Cyhoeddiad
2009
- Spurlock, G. et al. 2009. SPRED1 mutations (Legius syndrome): Another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype. Journal of Medical Genetics 46(7), pp. 431-437. (10.1136/jmg.2008.065474)
- Upadhyaya, M. et al. 2009. The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas. Neurogenetics 10(3), pp. 251-263. (10.1007/s10048-009-0178-0)
Articles
- Spurlock, G. et al. 2009. SPRED1 mutations (Legius syndrome): Another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype. Journal of Medical Genetics 46(7), pp. 431-437. (10.1136/jmg.2008.065474)
- Upadhyaya, M. et al. 2009. The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas. Neurogenetics 10(3), pp. 251-263. (10.1007/s10048-009-0178-0)