The long isoform of RUNX3 acts as a tumor supressor in human T-cell lymphoma

Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7

Comparative genomic hybridization of 20 patients with Sézary syndrome

Gene expression profiling of the Se-Ax cell line following E2A reconstitution

Genomic loss of the putative tumor suppressor gene E2A promotes cutaneous T-cell lymphoma in human

Screening for chromosomal aberrations by array CGH in 74 patients with congenital hypothyroidism

Array comparative genomic hybridization analysis of flat epithelial atypia (DIN1a) and lobular intraepithelial neoplasia

Positioning of Necrotic Lobular Intraepithelial Neoplasias within the sequence of breast carcinoma progression

Identification of Candidate Genes for Sporadic Amyotrophic Lateral Sclerosis by Array Comparative Genomic Hybridisation

Comparative genomic hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

Analysis of AML/MDS patients with 11q/MLL amplification

Mapping translocation breakpoints by next-generation sequencing

A defect in the ionotropic glutamate receptor 6 gene (GRIK2) causes autosomal recessive mental retardation

16p13 aberrations predispose to autism and MR

Array CGH in dendritic cell tumours

Array CGH in TAR syndrome

Array CGH in retinoblastoma

Array CGH in mentally retarded patients