• 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 genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease
• A highly complex rea(2;3;11) and aniridia by position effect
• 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 novel 4-cM minimally deleted region on chromosome 11p15.1 associated with high grade nonmucinous epithelial ovarian carcinomas
• A novel acquired cryptic three-way translocation t(2;11;5)(p21.3;q13.5;q23.2) with a submicroscopic deletion at 11p14.3 in an adult with hypereosinophilic syndrome
• A nude mouse Wilms' tumor line (KCMC-WT-1) derived from an aniridia patient with monoalleleic partial deletion of chromosome 11p
• Allele loss on chromosome 11q and microsatellite instability in malignant melanoma
• Allelic deletion at chromosome 11p13 defines a tumour suppressor region between the catalase gene and D11S935 in human non-small cell lung carcinoma
• Allelotyping of anaplastic thyroid carcinoma: frequent allelic losses on 1q, 9p, 11, 17, 19p, and 22q
• Analysis of loss of heterozygosity on chromosomes 10q, 11, and 16 in medulloblastomas
• Analysis of TSG101 tumour susceptibility gene transcripts in cervical and endometrial cancers
• Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?
• Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome
• ATM gene inactivation in mantle cell lymphoma mainly occurs by truncating mutations and missense mutations involving the phosphatidylinositol-3 kinase domain and is associated with increasing numbers of chromosomal imbalances
• Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y
• Brain-derived neurotrophic factor and obesity in the WAGR syndrome
• Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study
• Characteristic genomic imbalances in pediatric pheochromocytoma
• Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and FISH analysis
• Chromosomal mutations and chromosome loss measured in a new human-hamster hybrid cell line, ALC: studies with colcemid, ultraviolet irradiation, and 137Cs gamma-rays
• Chromosome 11 abnormalities in Bowen disease of the vulva
• Chromosome 11 allele imbalance and clinicopathological correlates in ovarian tumours
• Chromosome 1p and 11q deletions and outcome in neuroblastoma
• Clinical value of chromosome arms 19q and 11p losses in low-grade gliomas
• Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis
• Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype
• Combination of WAGR and Potocki-Shaffer contiguous deletion syndromes in a patient with an 11p11.2-p14 deletion
• Common genetic changes in hereditary and sporadic pituitary adenomas detected by comparative genomic hybridization
• Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology
• Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2
• Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia
• Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome
• Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor
• Correlation of novel PAX6 gene abnormalities in aniridia and clinical presentation
• CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
• Definition of a region of loss of heterozygosity at chromosome 11q in cervical carcinoma
• Del(5q) and MLL amplification in homogeneously staining region in acute myeloblastic leukemia: a recurrent cytogenetic association
• Deletion and duplication of 11p13-11p14: reciprocal aberrations derived from a paternal insertion
• Deletion of 11q23 is a frequent event in the evolution of MYCN single-copy high-risk neuroblastomas
• Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11
• Differential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridization
• DNA sequence losses on chromosomes 11p and 18q are associated with clinical outcome in lymph node-negative ductal breast cancer
• Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15
• Evaluation of chromosome 11p imbalances in aniridia and Wilms tumor patients
• Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumor of bone
• Facial dysostoses: Etiology, pathogenesis and management
• Factors affecting the timing and imprinting of replication on a mammalian chromosome
• Genetic abnormalities associated with nodal metastasis in head and neck cancer
• Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours
• Genetic changes observed in a case of adult pilocytic astrocytoma revealed by array CGH analysis
• Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas
• Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome
• High resolution allelotype of nonfunctional pancreatic endocrine tumors: identification of two molecular subgroups with clinical implications
• Human chromosome 11 suppresses the tumorigenicity of adenovirus transformed baby rat kidney cells: involvement of the Wilms' tumor 1 gene
• Human p57(KIP2) defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour
• Identification of 11p14.1-p15.3 deletion probably associated with short stature, relative macrocephaly, and delayed closure of the fontanelles
• Identification of a 6-cM minimal deletion at 11q23.1-23.2 and exclusion of PPP2R1B gene as a deletion target in cervical cancer
• Identification of a new commonly deleted region within a 2-cM interval of chromosome 11p11 in breast cancers
• Identification of a novel microsatellite marker tightly linked to the KAI-1 gene for predicting prostate cancer progression
• Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH
• Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p
• Interstitial deletion of 11(p11.2p12): a newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2)
• Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24)
• Localization of putative tumor suppressor loci by genome-wide allelotyping in human pancreatic endocrine tumors
• Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors
• Loss of heterozygosity of chromosome 8p and 11p in the dysplastic nodule and hepatocellular carcinoma
• Loss of heterozygosity on chromosome arms 5q, 11p, 11q, 13q, and 16p in human testicular germ cell tumors
• Lower expression of ATM and gene deletion is more frequent in adrenocortical carcinomas than adrenocortical adenomas
• Major form of NUP98/HOXC11 fusion in adult AML with t(11;12)(p15;q13) translocation exhibits aberrant trans-regulatory activity
• Measuring the spectrum of mutation induced by nitrogen ions and protons in the human-hamster hybrid cell line A(L)C
• Microsatellite alterations at 5q21, 11p13, and 11p15.5 do not predict survival in non-small cell lung cancer
• Microsatellite instability and loss of heterozygosity in primary breast tumours
• Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p
• Modifications of the antioxidant enzymes in relation to chromosome imbalances in human melanoma cell lines
• Molecular and clinical examination of an Italian DEFECT11 family
• Molecular characterization of the Yp11.2 region deletion in the Chinese Han population
• Molecular cytogenetic analysis of Spitz nevi shows clear differences to melanoma
• Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas
• Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
• Multiple chromosomal aberrations and 11p allelotyping in lung cancer cell lines
• Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion
• Mutations/deletions of the WT1 gene, loss of heterozygosity on chromosome arms 11p and 11q, chromosome ploidy and histology in Wilms' tumors in Japan
• Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)
• Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome
• Promiscuous translocations of chromosome arm 17q in human neuroblastomas
• Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects
• Proximal chromosome 11p contiguous gene deletion syndrome phenotype: case report and review of the literature
• Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis
• Smoking, gender, and survival association with allele loss for the LOH11B lung cancer region on chromosome 11
• SNP-based arrays complement classic cytogenetics in the detection of chromosomal aberrations in Wilms' tumor
• Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families
• Structural analysis of gene marker loci on chromosomes 10 and 11 in primary and secondary uraemic hyperparathyroidism
• The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)
• The oculocerebrorenal syndrome of Lowe: an update
• Toward a Molecular-Genetic Classification of Spitzoid Neoplasms
• WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion
• WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities