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Increasing the diagnostic yield of exome sequencing by copy number variant analysis.
Marchuk DS, Crooks K, Strande N, Kaiser-Rogers K, Milko LV, Brandt A, Arreola A, Tilley CR, Bizon C, Vora NL, Wilhelmsen KC, Evans JP, Berg JS. Marchuk DS, et al. Among authors: kaiser rogers k. PLoS One. 2018 Dec 17;13(12):e0209185. doi: 10.1371/journal.pone.0209185. eCollection 2018. PLoS One. 2018. PMID: 30557390 Free PMC article.
Co-occurring Down syndrome and SUCLA2-related mitochondrial depletion syndrome.
Couser NL, Marchuk DS, Smith LD, Arreola A, Kaiser-Rogers KA, Muenzer J, Pandya A, Gucsavas-Calikoglu M, Powell CM. Couser NL, et al. Among authors: kaiser rogers ka. Am J Med Genet A. 2017 Oct;173(10):2720-2724. doi: 10.1002/ajmg.a.38351. Epub 2017 Jul 27. Am J Med Genet A. 2017. PMID: 28749033
Lymphomas with pseudo-double-hit BCL6-MYC translocations due to t(3;8)(q27;q24) are associated with a germinal center immunophenotype, extranodal involvement, and frequent BCL2 translocations.
Johnson SM, Umakanthan JM, Yuan J, Fedoriw Y, Bociek RG, Kaiser-Rogers K, Sanmann JN, Montgomery ND. Johnson SM, et al. Among authors: kaiser rogers k. Hum Pathol. 2018 Oct;80:192-200. doi: 10.1016/j.humpath.2018.06.006. Epub 2018 Jun 11. Hum Pathol. 2018. PMID: 29902576
Prenatal diagnosis of mosaic complete trisomy 1q.
Schmitt CL, Moldenhauer JS, Wolfe H, Kaiser-Rogers K, Powell CM. Schmitt CL, et al. Am J Med Genet A. 2009 Aug;149A(8):1801-5. doi: 10.1002/ajmg.a.32986. Am J Med Genet A. 2009. PMID: 19610082 No abstract available.
30 results