Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2023 | 1 |
2024 | 2 |
Search Results
3 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the PTCH1 Gene in BCNS.
Curr Issues Mol Biol. 2023 Jun 24;45(7):5293-5304. doi: 10.3390/cimb45070336.
Curr Issues Mol Biol. 2023.
PMID: 37504252
Free PMC article.
[Diagnosis of MECP2 duplication in a child and prenatally].
Bokor BA, Török D, Horváth E, László Z, Pál M, Szűcs P, Széll M.
Bokor BA, et al.
Orv Hetil. 2024 Jan 7;165(1):30-34. doi: 10.1556/650.2024.32956. Print 2024 Jan 7.
Orv Hetil. 2024.
PMID: 38189840
Hungarian.
Item in Clipboard
A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder.
Nagy N, Pál M, Nagy D, Bokor BA, Zimmermann A, Gellén B, Salamon A, Sztriha L, Klivényi P, Széll M.
Nagy N, et al. Among authors: bokor ba.
BMC Pediatr. 2024 Jan 15;24(1):47. doi: 10.1186/s12887-023-04509-w.
BMC Pediatr. 2024.
PMID: 38225558
Free PMC article.
Item in Clipboard
Cite
Cite