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Rare MYC-N11S germline mutation indicative of inherited breast cancer in a multigeneration family.
BMJ Case Rep. 2022 Nov 11;15(11):e251336. doi: 10.1136/bcr-2022-251336.
BMJ Case Rep. 2022.
PMID: 36368728
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.
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Integrating Optical Genome Mapping and Whole Genome Sequencing in Somatic Structural Variant Detection.
Budurlean L, Tukaramrao DB, Zhang L, Dovat S, Broach J.
Budurlean L, et al.
J Pers Med. 2024 Mar 9;14(3):291. doi: 10.3390/jpm14030291.
J Pers Med. 2024.
PMID: 38541033
Free PMC article.
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