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
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Integrating Optical Genome Mapping and Whole Genome Sequencing in Somatic Structural Variant Detection.
J Pers Med. 2024 Mar 9;14(3):291. doi: 10.3390/jpm14030291.
J Pers Med. 2024.
PMID: 38541033
Free PMC article.
Rare MYC-N11S germline mutation indicative of inherited breast cancer in a multigeneration family.
Budurlean L, Baker M, Broach J.
Budurlean L, et al.
BMJ Case Rep. 2022 Nov 11;15(11):e251336. doi: 10.1136/bcr-2022-251336.
BMJ Case Rep. 2022.
PMID: 36368728
Item in Clipboard
Mutational profile of endometrial hyperplasia and risk of progression to endometrioid adenocarcinoma.
Russo M, Newell JM, Budurlean L, Houser KR, Sheldon K, Kesterson J, Phaeton R, Hossler C, Rosenberg J, DeGraff D, Shuman L, Broach JR, Warrick JI.
Russo M, et al. Among authors: budurlean l.
Cancer. 2020 Jun 15;126(12):2775-2783. doi: 10.1002/cncr.32822. Epub 2020 Mar 18.
Cancer. 2020.
PMID: 32187665
Free article.
Item in Clipboard
Cite
Cite