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Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review

Taiwanese journal of obstetrics & gynecology, 2011-09, Vol.50 (3), p.331-338

2011

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UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia

Genes chromosomes & cancer, 2023-04, Vol.62 (4), p.202-209

2023

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Cytogenetic risk stratification of 417 patients with chronic myelomonocytic leukemia from a single institution

American journal of hematology, 2014-08, Vol.89 (8), p.813-818

2014

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Optimal Treatment Approaches to Intestinal Behçet's Disease Complicated by Myelodysplastic Syndrome: The KASID and KSBD Multicenter Study

Yonsei Medical Journal, 2024, 65(5), , pp.265-275

2024

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Issues arising from the prenatal diagnosis of some rare trisomy mosaics-the importance of cryptic fetal mosaicism

Prenatal diagnosis, 2004-07, Vol.24 (7), p.524-536

2004

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Cytogenetics in the management of myelodysplastic neoplasms (myelodysplastic syndromes, MDS): Guidelines from the groupe francophone de cytogénétique hématologique (GFCH)

Current research in translational medicine, 2023-10, Vol.71 (4), p.103409-103409, Article 103409

2023

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Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review

BMC medical genomics, 2019-12, Vol.12 (1), p.197-197, Article 197

2019

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The high frequency of the U2AF1 S34Y mutation and its association with isolated trisomy 8 in myelodysplastic syndrome in Asians, but not in Caucasians

Leukemia research, 2017-10, Vol.61, p.96-103

2017

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Clinicopathologic evaluation of cytopenic patients with isolated trisomy 8: a detailed comparison between idiopathic cytopenia of unknown significance and low-grade myelodysplastic syndrome

Leukemia & lymphoma, 2017-03, Vol.58 (3), p.569-577

2017

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Outcome of allogeneic hematopoietic stem cell transplantation in adult patients with acute myeloid leukemia harboring trisomy 8

Annals of hematology, 2017-03, Vol.96 (3), p.469-478

2017

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Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes

British journal of haematology, 2012-11, Vol.159 (3), p.311-321

2012

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AML with gain of chromosome 8 as the sole chromosomal abnormality (+8sole) is associated with a specific molecular mutation pattern including ASXL1 mutations in 46.8% of the patients

Leukemia research, 2015-03, Vol.39 (3), p.265-272

2015

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Increased glycosylphosphatidylinositol-anchored protein-deficient granulocytes define a benign subset of bone marrow failures in patients with trisomy 8

European journal of haematology, 2015-09, Vol.95 (3), p.230-238

2015

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Refractoriness of Intestinal Behçet's Disease with Myelodysplastic Syndrome Involving Trisomy 8 to Medical Therapies - Our Case Experience and Review of the Literature

Digestion, 2013-01, Vol.88 (4), p.217-221

2013

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Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis

Cytogenetic and genome research, 2016-01, Vol.150 (1), p.35-39

2016

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Behcet's disease associated with bone marrow failure in Korean patients: clinical characteristics and the association of intestinal ulceration and trisomy 8

Rheumatology (Oxford, England), 2008-08, Vol.47 (8), p.1228-1230

2008

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Collagenous fibroma (desmoplastic fibroblastoma) with trisomy 8 as the sole cytogenetic abnormality

Anticancer research, 2013-08, Vol.33 (8), p.3259-3262

2013

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High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

Leukemia, 2006-05, Vol.20 (5), p.840-846

2006

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Clinical Prognostic Factors in 86 Chinese Patients with Primary Myelodysplastic Syndromes and Trisomy 8: A Single Institution Experience

Yonsei Medical Journal, 2016, 57(2), , pp.358-364

2016

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Exome Sequencing of an Adult Pituitary Atypical Teratoid Rhabdoid Tumor

Frontiers in oncology, 2015-10, Vol.5 (Article 236), p.236

2015

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Acute Myelogenous Leukemia With Trisomy 8 and Concomitant Acquired Factor VII Deficiency

JIM - high impact case reports, 2019, Vol.7, p.2324709619872657-2324709619872657

2019

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Constitutional trisomy 8 and Behçet syndrome

American journal of medical genetics. Part A, 2009-05, Vol.149A (5), p.982-986

2009

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Persistence of a monosomic cell line in a fetus with mosaic trisomy 8

American journal of medical genetics. Part A, 2011-11, Vol.155 (11), p.2791-2794

2011

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Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review

UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia

Cytogenetic risk stratification of 417 patients with chronic myelomonocytic leukemia from a single institution

Optimal Treatment Approaches to Intestinal Behçet's Disease Complicated by Myelodysplastic Syndrome: The KASID and KSBD Multicenter Study

Issues arising from the prenatal diagnosis of some rare trisomy mosaics-the importance of cryptic fetal mosaicism

Cytogenetics in the management of myelodysplastic neoplasms (myelodysplastic syndromes, MDS): Guidelines from the groupe francophone de cytogénétique hématologique (GFCH)

Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies

Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review

The high frequency of the U2AF1 S34Y mutation and its association with isolated trisomy 8 in myelodysplastic syndrome in Asians, but not in Caucasians

Clinicopathologic evaluation of cytopenic patients with isolated trisomy 8: a detailed comparison between idiopathic cytopenia of unknown significance and low-grade myelodysplastic syndrome

Outcome of allogeneic hematopoietic stem cell transplantation in adult patients with acute myeloid leukemia harboring trisomy 8

Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes

Dyspoietic changes associated with hepatosplenic T-cell lymphoma are not a manifestation of a myelodysplastic syndrome: analysis of 25 patients

AML with gain of chromosome 8 as the sole chromosomal abnormality (+8sole) is associated with a specific molecular mutation pattern including ASXL1 mutations in 46.8% of the patients

Increased glycosylphosphatidylinositol-anchored protein-deficient granulocytes define a benign subset of bone marrow failures in patients with trisomy 8

Refractoriness of Intestinal Behçet's Disease with Myelodysplastic Syndrome Involving Trisomy 8 to Medical Therapies - Our Case Experience and Review of the Literature

Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis

Behcet's disease associated with bone marrow failure in Korean patients: clinical characteristics and the association of intestinal ulceration and trisomy 8

Collagenous fibroma (desmoplastic fibroblastoma) with trisomy 8 as the sole cytogenetic abnormality

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

Clinical Prognostic Factors in 86 Chinese Patients with Primary Myelodysplastic Syndromes and Trisomy 8: A Single Institution Experience

Exome Sequencing of an Adult Pituitary Atypical Teratoid Rhabdoid Tumor

Acute Myelogenous Leukemia With Trisomy 8 and Concomitant Acquired Factor VII Deficiency

Constitutional trisomy 8 and Behçet syndrome

Persistence of a monosomic cell line in a fetus with mosaic trisomy 8

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