• 11q- syndrome: three cases and a review of the literature
• A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum
• A case of Jacobsen syndrome with multifocal white matter lesions
• A de novo 0.57 Mb microdeletion in chromosome 11q13.1 in a patient with speech problems, autistic traits, dysmorphic features and multiple endocrine neoplasia type 1
• A Maternally Inherited Rare Case with Chromoanagenesis-Related Complex Chromosomal Rearrangements and De Novo Microdeletions
• Autotransplants in multiple myeloma: what have we learned?
• Characteristic pattern of chromosomal gains and losses in primary large B-cell lymphomas of the gastrointestinal tract
• Characterization of nonrandom chromosomal gains and losses in multiple myeloma by comparative genomic hybridization
• Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy
• Chromosomal rearrangements detected by FISH and G-banding
• Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case
• Clinical and Cytogenetic Characteristics of Two AML Patients with High-level MLL Expression
• Clinical and molecular-cytogenetic evaluation of a family with partial Jacobsen syndrome without thrombocytopenia caused by an approximately 5 Mb deletion del(11)(q24.3)
• Clinico-pathological impact of cytogenetic subgroups in B-cell chronic lymphocytic leukemia: experience from India
• Clonal chromosomal abnormalities as direct evidence for clonality in nasal T/natural killer cell lymphomas
• Coarctation of the aorta with aortic arch hypoplasia in newborn with partial trisomy 11q associated to 4q interstitial deletion
• Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findings
• Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk
• Comparison of different techniques for the detection of genetic risk-identifying chromosomal gains and losses in neuroblastoma
• Complex Mosaic Ring Chromosome 11 Associated with Hemizygous Loss of 8.6 Mb of 11q24.2qter in Atypical Jacobsen Syndrome
• Confirmation of a maternal cryptal balanced translocation through analysis of a fetus using microarray
• Copy number variation analysis on a non-Hodgkin lymphoma case-control study identifies an 11q25 duplication associated with diffuse large B-cell lymphoma
• Copy number variations could predict the outcome of bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma
• Cytogenetic profile of lymphoma of follicle mantle lineage: correlation with clinicobiologic features
• Cytogenetic profile of myelodysplastic syndromes with complex karyotypes: an analysis using spectral karyotyping
• Deletion of 11q12.3-11q13.1 in a patient with intellectual disability and childhood facial features resembling Cornelia de Lange syndrome
• Deletion of 11q23 is a frequent event in the evolution of MYCN single-copy high-risk neuroblastomas
• Design and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia
• Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)
• Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay
• Dissecting the role of TP53 alterations in del(11q) chronic lymphocytic leukemia
• Distal Deletion of Chromosome 11q Encompassing Jacobsen Syndrome without Platelet Abnormality
• Distinct patterns of chromosomal alterations in high- and low-grade head and neck squamous cell carcinomas
• Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
• FEVR-like Presentation in an 11q Deletion Syndrome and 16p13.11 Microdeletion
• Fluorescence in situ hybridization analyses of hematologic malignancies reveal frequent cytogenetically unrecognized 12p rearrangements
• Frequency, variations, and prognostic implications of chromosome 14q32 deletions in chronic lymphocytic leukemia
• Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1)
• Gain of chromosome 17 is the most frequent abnormality detected in neuroblastoma by comparative genomic hybridization
• GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma
• Genetic abnormalities in chronic lymphocytic leukemia and their clinical and prognostic implications
• Genetic changes in chronic lymphocytic leukemia
• Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization
• Genetics of familial forms of thrombocytopenia
• Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia
• Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 --> qter, and trisomy 8q24.3 --> qter
• High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH
• Human ependymomas reveal frequent deletions on chromosomes 6 and 9
• Hypoimmunoglobulinemia and protein C deficiency in a girl with Jacobsen syndrome: a case report
• Immune Deficiency in Jacobsen Syndrome: Molecular and Phenotypic Characterization
• Impact of Genomic and Clinical Factors on Outcome of Children ≥18 Months of Age with Stage 3 Neuroblastoma with Unfavorable Histology and without MYCN Amplification: A Children's Oncology Group (COG) Report
• Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array
• Interstitial 11q24 deletion: a new case and review of the literature
• Jacobsen and Beckwith-Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy
• Jacobsen syndrome
• Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24)
• Loss of distal 11q is associated with DNA repair deficiency and reduced sensitivity to ionizing radiation in head and neck squamous cell carcinoma
• Mantle cell lymphomas with clonal immunoglobulin V(H)3-21 gene rearrangements exhibit fewer genomic imbalances than mantle cell lymphomas utilizing other immunoglobulin V(H) genes
• Microarray-based comparative genomic hybridization of pheochromocytoma cell lines from neurofibromatosis knockout mice reveals genetic alterations similar to those in human pheochromocytomas
• Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura
• Molecular cytogenetic characterization of marginal zone B-cell lymphoma: correlation with clinicopathologic findings in 14 cases
• Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies
• Molecular studies of segmental aneusomy: FISHing for the atypical cry in del(5)(p15.3)
• Monosomy 11Q: report of new phenotypic manifestations
• Morphological and genetic abnormalities in a Jacobsen syndrome
• Multicentre analysis of patterns of DNA gains and losses in 204 neuroblastoma tumors: how many genetic subgroups are there?
• Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping
• Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis
• Partial allelotype of carcinoma in situ of the human bladder
• Partial deletion 11q: report of a case with a large terminal deletion 11q21-qter without loss of telomeric sequences, and review of the literature
• Partial deletion of the long arm of chromosome 11: ten Japanese children
• Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation
• Partial monosomy 10q with partial trisomy 11q due to paternal balanced translocation
• Partial monosomy 11q and trisomy 12q: variable expression in two siblings
• Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delay
• Partial trisomy 11q and partial monosomy 12p due to the maternal translocation (11q;12p)
• Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report
• Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report
• Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature
• Phenotypic correction of ataxia-telangiectasia cellular defect by exogenously introduced human or mouse subchromosomal fragments
• Poor prognosis in multiple myeloma is associated only with partial or complete deletions of chromosome 13 or abnormalities involving 11q and not with other karyotype abnormalities
• Prenatal diagnosis of a case with combined Wolf-Hirschhorn syndrome and Jacobsen syndrome
• Prenatal diagnosis of mosaicism for 11q terminal deletion
• Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly
• Prenatal Identification and Confirmation of Jacobsen Syndrome: A Series of Four Cases
• Prognostic value of partial genetic instability in neuroblastoma with ≤50% neuroblastic cell content
• Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11q
• Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells
• Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: molecular characterization of two der(11)t(11;16)
• Ten-year use of recombinant parathyroid hormone for the treatment of hypoparathyroidism in a boy with partial Jacobsen syndrome
• Terminal deletion 6q syndrome with 11q partial trisomy mosaicism due to maternal balanced translocation
• Terminal deletion of 11q with significant late-onset combined immune deficiency
• The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency
• The combination of rituximab, bendamustine, and cytarabine for heavily pretreated relapsed/refractory cytogenetically high-risk patients with chronic lymphocytic leukemia
• Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up
• Two craniosynostotic patients with 11q deletions, and review of 48 cases
• Unbalanced translocation der(7)t(7q;11q): a new recurrent aberration leading to partial monosomy 7q and trisomy 11q in acute myeloid leukemia
• Unique role of cytogenetics in the prognosis of patients with myeloma receiving high-dose therapy and autotransplants
• Velopharyngeal insufficiency, submucous cleft palate and a phonological disorder as the associated clinical features which led to the diagnosis of Jacobsen syndrome. Case report and review of the literature
• Ventriculomegaly and cerebellar hypoplasia in a neonate with interstitial 11q 24 deletion in Jacobsen syndrome region