• 11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia
• 50 Years Ago in TheJournalofPediatrics: Understanding the Molecular Basis of 11p13 Deletion
• A familial pericentric inversion of chromosome 11 associated with a microdeletion of 163 kb and microduplication of 288 kb at 11p13 and 11q22.3 without aniridia or eye anomalies
• A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)
• A nude mouse Wilms' tumor line (KCMC-WT-1) derived from an aniridia patient with monoalleleic partial deletion of chromosome 11p
• A partial allelotyping of urothelial carcinoma of bladder in the Chinese
• A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations
• Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome
• Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y
• Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis
• Chromosomal abnormalities associated with omphalocele
• Chromosome abnormalities in tumor cells from patients with sporadic Wilms' tumor
• Clonal and chronological genetic analysis of multifocal cancers of the bladder and upper urinary tract
• CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
• Deletion of 11q23 is a frequent event in the evolution of MYCN single-copy high-risk neuroblastomas
• Efficient immortalization by SV40 T DNA of skin fibroblasts from patients with Wilms' tumor associated with chromosome 11p deletion
• Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15
• From cytogenetics to cytogenomics of bladder cancers
• Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes
• Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH
• Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24)
• Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes
• Molecular cytogenetics of human papillomavirus-negative cervical carcinoma cell lines
• Molecular screening of pituitary adenomas for gene mutations and rearrangements
• Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping
• Partial allelotype of carcinoma in situ of the human bladder
• Partial deletion of chromosome 11p in breast cancer correlates with size of primary tumour and oestrogen receptor level
• Polymerase chain reaction allelotyping of human ovarian cancer
• Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome
• SNP-based arrays complement classic cytogenetics in the detection of chromosomal aberrations in Wilms' tumor
• The gene for catalase is assigned between the antigen loci MIC4 and MIC11
• The genetic architecture of aniridia and Gillespie syndrome
• Unbalanced translocation of chromosome 3p in Wilms' tumor
• Unique secondary chromosomal abnormalities are frequently found in the chronic phase of chronic myeloid leukemia in southern Vietnam
• WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion