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Cytogenetic characterization of the malignant primitive neuroectodermal SK-PN-DW tumor cell line

BMC cancer, 2019-05, Vol.19 (1), p.412-412, Article 412

2019

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Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies

Molecular cytogenetics, 2022-04, Vol.15 (1), p.17-17, Article 17

2022

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Methylation of SPRED1: A New Target in Acute Myeloid Leukemia

Frontiers in oncology, 2022-03, Vol.12, p.854192-854192

2022

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Genomic Copy Number Variants in CML Patients With the Philadelphia Chromosome (Ph+): An Update

Frontiers in genetics, 2021-08, Vol.12, p.697009-697009

2021

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Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review

Molecular cytogenetics, 2020-08, Vol.13 (1), p.37-37, Article 37

2020

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SPRED1 Is Downregulated and a Prognostic Biomarker in Adult Acute Myeloid Leukemia

Frontiers in oncology, 2020-02, Vol.10, p.204-204

2020

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Identification of novel genomic aberrations in AML-M5 in a level of array CGH

PloS one, 2014-04, Vol.9 (4), p.e87637-e87637

2014

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Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: Microcephaly, developmental delay and delayed bone age

American journal of medical genetics. Part A, 2011-06, Vol.155 (6), p.1374-1378

2011

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Transplantation of bone marrow cells from miR150 knockout mice improves senescence-associated humoral immune dysfunction and arterial stiffness

Metabolism, clinical and experimental, 2022-09, Vol.134, p.155249-155249, Article 155249

2022

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Feature Selection for the Automated Detection of Metaphase Chromosomes: Performance Comparison Using a Receiver Operating Characteristic Method

Analytical cellular pathology (Amsterdam), 2014-01, Vol.2014 (2014), p.1-9

2014

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Automated Analysis of Fluorescent in situ Hybridization (FISH) Labeled Genetic Biomarkers in Assisting Cervical Cancer Diagnosis

Technology in cancer research & treatment, 2010-06, Vol.9 (3), p.231-242

2010

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eP179 - Characterization of partial trisomy chromosome 11q in a patient with congenital anomalies and literature review

Molecular genetics and metabolism, 2021-04, Vol.132, p.S117-S117

2021

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Characterization of partial trisomy chromosome 11q in a patient with congenital anomalies and literature review

Molecular genetics and metabolism, 2021-04, Vol.132, p.S117

2021

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Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation

Journal of biomedical optics, 2022-01, Vol.27 (1), p.016504-016504

2022

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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

Arthritis & rheumatology (Hoboken, N.J.), 2016-05, Vol.68 (5), p.1290-1300

2016

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Identification of a cryptic submicroscopic deletion using a combination of fluorescence in situ hybridization and array comparative genomic hybridization in a t(3;5)(q25;q35)-positive acute myeloid leukemia patient: A case report and review of the literature

Medicine (Baltimore), 2020-10, Vol.99 (43), p.e22789-e22789

2020

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Simultaneous involvement of 11q23 translocation resulting in chimeric MLL-AFF1 and a second translocation [t (9;21) (p13; p11.2)] in an infant acute lymphoblastic leukemia patient at relapse: A case report

Medicine (Baltimore), 2018-05, Vol.97 (21), p.e10874

2018

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X Chromosome Dose and Sex Bias in Autoimmune Diseases

Arthritis & rheumatology (Hoboken, N.J.), 2016, Vol.68 (5), p.1290

2016

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FLT3 Amplification as Double Minute Chromosomes in a Patient with Chronic Myelomonocytic Leukemia

Disease markers, 2021, Vol.2021, p.1-6

2021

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Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization

Scientific reports, 2017-09, Vol.7 (1), p.10395-9, Article 10395

2017

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Infantile Epithelioid Sarcoma with Genomic Segmental Amplification of BIRC3/YAP1 as Double Minutes Plus Trisomy 2: A Case Report

Fetal and pediatric pathology, 2020-01, Vol.39 (1), p.51-61

2020

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Coexistence of t(2;14;11)(p16.1;q32;q23) and t(14;19)(q32;q13.3) chromosome translocations in a patient with chronic lymphocytic leukemia: A case report

Medicine (Baltimore), 2017-12, Vol.96 (51), p.e9169

2017

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Two patients with small chromosome 22q11.21 alterations and central nervous system abnormalities

Molecular cytogenetics, 2015-12, Vol.8 (105), p.102, Article 102

2015

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An extra chromosome 9 derived from either a normal chromosome 9 or a derivative chromosome 9 in a patient with acute myeloid leukemia positive for t(9;11)(p21.3;q23.3): A case report

Oncology letters, 2019-12, Vol.18 (6), p.6725-6731

2019

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Chromothripsis and Chromosomal Rearrangements in an Adult Patient With Acute Lymphocytic Leukemia

Cancer genetics, 2017-08, Vol.214, p.49-49

2017

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Cytogenetic characterization of the malignant primitive neuroectodermal SK-PN-DW tumor cell line

Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies

Methylation of SPRED1: A New Target in Acute Myeloid Leukemia

Genomic Copy Number Variants in CML Patients With the Philadelphia Chromosome (Ph+): An Update

Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review

SPRED1 Is Downregulated and a Prognostic Biomarker in Adult Acute Myeloid Leukemia

Identification of novel genomic aberrations in AML-M5 in a level of array CGH

Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: Microcephaly, developmental delay and delayed bone age

Transplantation of bone marrow cells from miR150 knockout mice improves senescence-associated humoral immune dysfunction and arterial stiffness

Feature Selection for the Automated Detection of Metaphase Chromosomes: Performance Comparison Using a Receiver Operating Characteristic Method

Automated Analysis of Fluorescent in situ Hybridization (FISH) Labeled Genetic Biomarkers in Assisting Cervical Cancer Diagnosis

eP179 - Characterization of partial trisomy chromosome 11q in a patient with congenital anomalies and literature review

Characterization of partial trisomy chromosome 11q in a patient with congenital anomalies and literature review

Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation

X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

Identification of a cryptic submicroscopic deletion using a combination of fluorescence in situ hybridization and array comparative genomic hybridization in a t(3;5)(q25;q35)-positive acute myeloid leukemia patient: A case report and review of the literature

Simultaneous involvement of 11q23 translocation resulting in chimeric MLL-AFF1 and a second translocation [t (9;21) (p13; p11.2)] in an infant acute lymphoblastic leukemia patient at relapse: A case report

X Chromosome Dose and Sex Bias in Autoimmune Diseases

FLT3 Amplification as Double Minute Chromosomes in a Patient with Chronic Myelomonocytic Leukemia

Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization

Infantile Epithelioid Sarcoma with Genomic Segmental Amplification of BIRC3/YAP1 as Double Minutes Plus Trisomy 2: A Case Report

Coexistence of t(2;14;11)(p16.1;q32;q23) and t(14;19)(q32;q13.3) chromosome translocations in a patient with chronic lymphocytic leukemia: A case report

Two patients with small chromosome 22q11.21 alterations and central nervous system abnormalities

An extra chromosome 9 derived from either a normal chromosome 9 or a derivative chromosome 9 in a patient with acute myeloid leukemia positive for t(9;11)(p21.3;q23.3): A case report

Chromothripsis and Chromosomal Rearrangements in an Adult Patient With Acute Lymphocytic Leukemia

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