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Patients with telomere biology disorders show context specific somatic mosaic states with high frequency of U2AF1 variants.
Am J Hematol. 2023 Dec;98(12):E357-E359. doi: 10.1002/ajh.27086. Epub 2023 Sep 4.
Am J Hematol. 2023.
PMID: 37665761
Clinical and molecular correlates of somatic and germline DDX41 variants in patients and families with myeloid neoplasms.
Badar T, Nanaa A, Foran JM, Viswanatha D, Al-Kali A, Lasho T, Finke C, Alkhateeb HB, He R, Gangat N, Shah M, Tefferi A, Mangaonkar AA, Litzow MR, Ongie LJ, Chlon T, Ferrer A, Patnaik MM.
Badar T, et al. Among authors: ongie lj.
Haematologica. 2023 Nov 1;108(11):3033-3043. doi: 10.3324/haematol.2023.282867.
Haematologica. 2023.
PMID: 37199125
Free PMC article.
Review.
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Pediatric manifestations of Lynch Syndrome: A single center experience.
MacArthur TA, Ongie LJ, Lanpher BC, Ishitani MB.
MacArthur TA, et al. Among authors: ongie lj.
J Pediatr Surg Case Rep. 2022 Nov;86:102431. doi: 10.1016/j.epsc.2022.102431. Epub 2022 Aug 26.
J Pediatr Surg Case Rep. 2022.
PMID: 36313796
Free PMC article.
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Neurofibromatosis 1 in the setting of dual diagnosis: Diagnostic and management conundrums.
Muthusamy K, El-Jabali A, Ongie LJ, Dhamija R, Babovic-Vuksanovic D.
Muthusamy K, et al. Among authors: ongie lj.
Am J Med Genet A. 2022 Mar;188(3):911-918. doi: 10.1002/ajmg.a.62575. Epub 2021 Nov 19.
Am J Med Genet A. 2022.
PMID: 34797032
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