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 | 2 |
2024 | 1 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Delayed-onset adenosine deaminase deficiency with a novel synonymous mutation and a case series from China.
World J Pediatr. 2023 Jul;19(7):687-700. doi: 10.1007/s12519-023-00729-3. Epub 2023 May 8.
World J Pediatr. 2023.
PMID: 37154862
X-linked chronic granulomatous disease secondary to skewed X-chromosome inactivation in female patients.
Zhang Y, Shu Z, Li Y, Piao Y, Sun F, Han T, Wang T, Mao H.
Zhang Y, et al.
Clin Exp Immunol. 2024 Feb 19;215(3):261-267. doi: 10.1093/cei/uxad129.
Clin Exp Immunol. 2024.
PMID: 38066563
Item in Clipboard
Progressive osseous heteroplasia in a 5-year-old boy with a novel mutation in exon 2 of GNAS: a case presentation and literature review.
Ma J, Mo W, Sun J, Li Y, Han T, Mao H.
Ma J, et al.
BMC Musculoskelet Disord. 2023 Mar 31;24(1):247. doi: 10.1186/s12891-023-06371-4.
BMC Musculoskelet Disord. 2023.
PMID: 37003989
Free PMC article.
Item in Clipboard
Cite
Cite