array comparative genomic hybridization (aCGH)
Genomic profiling using array comparative genomic hybridization define distinct subtypes of diffuse large b-cell lymphoma: a review of the literature
12
Array Comparative Genomic Hybridization as a Diagnostic Tool in Cancer
7
Array comparative genomic hybridization of 18 pancreatic ductal adenocarcinomas and their autologous metastases
9
Well differentiated angiosarcoma of spleen: a teaching case mimicking hemagioma and cytogenetic analysis with array comparative genomic hybridization
6
Establishment of a new human osteosarcoma cell line, UTOS-1: cytogenetic characterization by array comparative genomic hybridization
8
Chromosomal Aberrations in ETV6/RUNX1-positive Childhood Acute Lymphoblastic Leukemia using 244K Oligonucleotide Array Comparative Genomic Hybridization
6
Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization
6
A 18p11.23-p11.31 microduplication in a boy with psychomotor delay, cerebellar vermis hypoplasia, chorioretinal coloboma, deafness and GH deficiency
6
Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series
12
Preimplantation genetic diagnosis guided by single-cell genomics
10
Molecular cytogenetic characterization of undifferentiated embryonal sarcoma of the liver: a case report and literature review
8
Yield of comparative genomic hybridization microarray in pediatric neurology practice
11
Genomic scars as biomarkers of homologous recombination deficiency and drug response in breast and ovarian cancers
11
Application of next-generation sequencing for 24-chromosome aneuploidy screening of human preimplantation embryos
9
Array-CGH characterization and genotype-phenotype analysis in a patient with a ring chromosome 6
7
Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities
5
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome – case report and review of the literature
8
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature
7
Application of Array Based Comparative Genomic Hybridization to Pediatric Neurologic Diseases
7
Genetic analysis of products of conception using a HLPA/SNP-array strategy
7