Copy number profiling of 556 high-risk neuroblastoma patients using aCGH or SNP arrays

Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephaly

Experiment to determine DNA copy number of the HCE-T cell line relative to normal duploid cell

Investigation of a patient with a partial 16q trisomy

Agilent 244A aCGH array for comparison of lung tumor CNA to high-throughput sequencing data

aCGH hybridization of breast cancer cell line T47D

Molecular Cytogenetic Analysis of a Gliosarcoma with Osseous Metaplasia

Ten percent of aberrant cells is sufficient for detection of DNA copy number alterations (part 4)

Ten percent of aberrant cells is sufficient for detection of DNA copy number alterations (part 5)

Oligo array for calling CNV's for AUTS2 project [NimbleGen]

Oligo array for CNV calling AUTS2 project [Bluegnome]

SNP array data for embryonal rhabdomyosarcoma in a patient with Costello syndrome

Variant acute promyelocytic leukemia (APL) bone marrow aCGH

The genomic landscape of small intestine neuroendocrine tumors [CGH]

A large novel deletion downstream of PAX6 gene in a Chinese family with coloboma of iris

Identification of CNA associated with bone metastatic breast cancer cells

Cell cycle and P53 gate the direct conversion of human fibroblasts to dopaminergic neurons

SMC2: a candidate gene associated with Cornelia de Lange Syndrome

Novel type of EATL evolving from mucosal γδ-T-cells in a RCD type I patient

Application of array-CGH for the detection of genomic rearrangements responsible for syndromic mental retardation of unknown cause