Lv11
35 积分 2020-12-07 加入
Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1
6小时前
待确认
NF1 mutations in neurofibromatosis 1 patients with plexiform neurofibromas
6小时前
已完结
Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1
6小时前
已完结
Functional assessment of TSC2 variants identified in individuals with tuberous sclerosis complex
8天前
已完结
SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T)
22天前
已完结
Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features
22天前
已关闭
Juxtamembrane autoinhibition in receptor tyrosine kinases
1个月前
已完结
Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutations
1个月前
已完结
Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients
2个月前
已完结
Pediatric glioblastoma in the setting of constitutional mismatch-repair deficiency treated with upfront lomustine and nivolumab
2个月前
已完结
皖公网安备34019202002308
