Last Updated: 09/26/2026
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Found 17 publications
Structural complexity and mechanistic diversity of MECOM rearrangements in myeloid neoplasms.
Journal: Pathology
Published: December 23, 2025
Correction: Case Report: Unraveling complex genomic alterations in a case of chronic lymphocytic leukemia using optical genome mapping.
Journal: Frontiers in oncology
Published: September 17, 2025
Case Report: Unraveling complex genomic alterations in a case of chronic lymphocytic leukemia using optical genome mapping.
Journal: Frontiers in oncology
Published: June 02, 2025
Effects of platforms, size filter cutoffs, and targeted regions of cytogenomic microarray on detection of copy number variants and uniparental disomy in prenatal diagnosis: Results from 5026 pregnancies.
Journal: Prenatal diagnosis
Published: February 22, 2018
Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysis.
Journal: Molecular cytogenetics
Published: August 24, 2016
Chromosomal microarray analysis as the first-tier test for the identification of pathogenic copy number variants in chromosome 9 pericentric regions and its challenge.
Journal: Molecular cytogenetics
Published: July 12, 2016
Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS).
Journal: PloS one
Published: April 05, 2016
Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHD.
Journal: Neuromuscular disorders : NMD
Published: May 26, 2015
Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features.
Journal: American journal of medical genetics. Part A
Published: July 10, 2014
Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 28, 2014
Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay.
Journal: Molecular cytogenetics
Published: March 13, 2014
Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory.
Journal: Molecular cytogenetics
Published: February 21, 2014
Last Updated: 09/26/2026