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der(1)t(1;1)(p36;q10) as a Rare Variant of 1q Gain in Fanconi Anemia-Associated Myelodysplastic Syndrome
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참고문헌 (9)
- Cioc AM, "Diagnosis of myelodysplastic syndrome among a cohort of 119 patients with Fanconi anemia: morphologic and cytogenetic characteristics", Am J Clin Pathol, 132, pp.92~100 (2010)
- van de Vrugt HJ, "Effective CRISPR", Cas9-mediated correction of a Fanconi anemia defect by error-prone end joining or templated repair, 2019, pp.9, 768~
- Quentin S, "Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1", AML1 lesions, 2011, pp.177, e161~e170
- Kristin Karner, "Current Aspects of Clonal Hematopoiesis: Implications for Clinical Diagnosis", Annals of Laboratory Medicine, 39(6), pp.509~514 (2019), 대한진단검사의학회[DOI]
- Zamecnikova A, "der(1)t(1;1)(p36;q11-q32) in hematopoietic malignancies", Atlas Genet Cytogenet Oncol Haematol, 21, pp.150~155 (2017)
- de Latour RP, "How I treat MDS and AML in Fanconi anemia", Blood, 127, pp.2971~2979 (2016)
- Fu B, "Bone marrow fibrosis in patients with primary myelodysplastic syndromes has prognostic value using current therapies and new risk stratification systems", Mod Pathol, 27, pp.681~689 (2014)
- Della Porta MG, "Minimal morphological criteria for defining bone marrow dysplasia: a basis for clinical implementation of WHO classification of myelodysplastic syndromes", Leukemia, 29, pp.66~75 (2015)
- Duhoux FP, "PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies", Br J Haematol, 156, pp.76~88 (2012)
관련 논문AI추천
A Rare Case of Primary Myelofibrosis With a Solitary 1q Triplication김덕언, Jin-Hong Kim, Young-Eun Kim대한진단검사의학회 · Annals of Laboratory Medicine2020 · 제40권 제2호Cryptic e1a2 BCR-ABL1 Fusion With Complex Chromosomal Abnormality in de novo Myelodysplastic Syndrome강민구, 김수현, 서보영, 서순팔, 신명근, 신종희, 양동욱, 이준형, 최석용대한진단검사의학회 · Annals of Laboratory Medicine2015 · 제35권 제6호A Case of Near-triploidy in Myelodysplastic Syndrome with del(5q) Combined with del(1p) and del(13q)김경희, 한진영, Bo-Ram Kim, Jeong-Man Kim, Ji-Eun Kim, Kwang-Sook Woo, Lisa G. Shaffer, Suee Lee대한진단검사의학회 · Annals of Laboratory Medicine2012 · 제32권 제4호The First Case of Acute Myeloid Leukemia With a Novel Five-way Variant Translocation of RUNX1–RUNX1T1장미애, Han Eun-Ae, Jeon Byung Ryul, Jo Yong Hun, Park Seong Kyu대한진단검사의학회 · Annals of Laboratory Medicine2023 · 제43권 제3호Myelodysplasia-Related Features of Acute Myeloid Leukemia Evolving From Philadelphia-Negative Myeloproliferative Neoplasms김보현, 박찬정, 배미현, 서을주, 장성수, 조영욱, 지현숙, Jae Ryuk Kim대한진단검사의학회 · Annals of Laboratory Medicine2016 · 제36권 제4호Rare Gene Rearrangement t(11;22)(q23;q13)/ KMT2A-EP300 in Therapy-related Acute Myeloid Leukemia: A Case ReportKim Seo Wan, Lee Seungjae, Lee Seung-Tae, Shin Saeam대한진단검사의학회 · Annals of Laboratory Medicine2022 · 제42권 제6호
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