Order results by:
Issue | Title | |
Vol 10, No 1S (2018): СПЕЦВЫПУСК: ЭПИЛЕПСИЯ | A clinical case of SYNGAP1-associated encephalopathy in a girl with epilepsy, intellectual disability, and autism | Abstract similar documents |
N. N. Savelieva, A. V. Yakunina, I. E. Poverennova | ||
"... in differential diagnosis, since in addition to SYNGAP1 mutation (c2214_2217deltgag), heterozygous BCKDHB gene ..." | ||
1 - 1 of 1 Items |
Search tips:
- Search terms are case-insensitive
- Common words are ignored
- By default articles containing any term in the query are returned (i.e., OR is implied)
- Make sure that a word exists in an article by prefixing it with +; e.g., +journal +access scholarly academic
- Combine multiple words with AND to find articles containing all terms; e.g., education AND research
- Exclude a word by prefixing it with - or NOT; e.g., online -politics or online NOT politics
- Search for an exact phrase by putting it in quotes; e.g., "open access publishing". Hint: Quoting Chinese or Japanese words will help you to find exact word matches in mixed-language fields, e.g. "中国".
- Use parentheses to create more complex queries; e.g., archive ((journal AND conference) NOT theses)