Disease: Chromosome 11- partial trisomy 11q
- 'Pure' partial trisomy 11q (11q23.1→11qter): expanding the phenotype
- A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome
- A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review
- A large fraction of trisomy 12, 17p<sup>-</sup>, and 11q<sup>-</sup> CLL cases carry unidentified microdeletions of <em>miR-15a/16-1</em>
- A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature
- A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report
- A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21
- A unique lethal blastoid transformation of B-cell chronic lymphocytic leukemia carrying ATM/11q deletion and trisomy 12
- An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma
- Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor
- Characterizing patients with multiple chromosomal aberrations detected by FISH in chronic lymphocytic leukemia
- Chemoimmunotherapy may overcome the adverse prognostic significance of 11q deletion in previously untreated patients with chronic lymphocytic leukemia
- Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenström's macroglobulinemia
- Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case
- Chromosome aberrations in B-cell chronic lymphocytic leukemia: reassessment based on molecular cytogenetic analysis
- Chromosome abnormalities in juxtaglomerular cell tumors
- Clinical, immunophenotypic, and molecular profiling of trisomy 12 in chronic lymphocytic leukemia and comparison with other karyotypic subgroups defined by cytogenetic analysis
- Clonal selection of 11q CN-LOH and CBL gene mutation in a serially studied patient during MDS progression to AML
- 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
- Complex analysis of prognostic factors in chronic lymphocytic leukemia
- Confirmation of a maternal cryptal balanced translocation through analysis of a fetus using microarray
- Congenital diaphragmatic hernia associated with duplication of 11q23-qter
- Constitutional duplication 11q23 de novo involving the MLL gene
- Contribution of comparative genomic hybridization and fluorescence in situ hybridization to the detection of chromosomal abnormalities in B-cell chronic lymphocytic leukemia
- Copy number variation analysis on a non-Hodgkin lymphoma case-control study identifies an 11q25 duplication associated with diffuse large B-cell lymphoma
- Correlation between cytogenetic abnormalities and disease characteristics in multiple myeloma: monosomy of chromosome 13 and structural abnormalities of 11q are associated with a high percentage of S-phase plasma cells
- Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocation
- Cyclin D1 overexpression is a favorable prognostic variable for newly diagnosed multiple myeloma patients treated with high-dose chemotherapy and single or double autologous transplantation
- Cytogenetic findings in two new cases of hepatoblastoma
- Cytogenetic manifestation of chromosome 11 duplication/amplification in acute myeloid leukemia
- Cytogenetic profile of lymphoma of follicle mantle lineage: correlation with clinicobiologic features
- Developmental retardation due to paternal 5q/11q translocation in a Chinese infant: clinical, chromosomal and microarray characterization
- Familial interstitial duplication of 11q; partial trisomy (11)(q13.5q21)
- Fatal Outcome in a Newborn Calf Associated with Partial Trisomy 25q and Partial Monosomy 11q, 60,XX,der(11)t(11;25)(q11;q14∼21)
- Favorable outcome of triploid neuroblastomas: a contribution to the special oncogenesis of neuroblastoma
- FISH analyses for alterations in chromosomes 1, 2, 3, and 11 define high-risk groups in neuroblastoma
- Fulminant blast crisis with de novo 11q23 rearrangement in a Philadelphia-positive CML patient undergoing treatment with dasatinib
- 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 11q by an additional ring chromosome 11 and trisomy 18 in CD5-positive intravascular large B-cell lymphoma
- Genetics and risk-stratified approach to therapy in chronic lymphocytic leukemia
- 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
- High incidence of trisomies 1q, 9q, and 11q in multiple myeloma: results from a comprehensive molecular cytogenetic analysis
- High rate of neoplastic cells with genetic abnormalities in proliferation centers of chronic lymphocytic leukemia
- Identification and molecular characterization of a small 11q23.3 de novo duplication in a patient with Rett syndrome manifestations
- Impact of trisomy 12, del(13q), del(17p), and del(11q) on the immunophenotype, DNA ploidy status, and proliferative rate of leukemic B-cells in chronic lymphocytic leukemia
- Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array
- In vitro activity of 20 agents in different prognostic subgroups of chronic lymphocytic leukemia--rolipram and prednisolone active in cells from patients with poor prognosis
- Inconsistency of omphalocoele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q
- IS THE AMPLIFICATION OF c-MYC, MLL AND RUNX1 GENES IN AML AND MDS PATIENTS WITH TRISOMY 8, 11 AND 21 A FACTOR FOR A CLONAL EVOLUTION IN THEIR KARYOTYPE?
- Jacobsen and Beckwith-Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy
- Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24)
- Jumping translocations involving 11q in a non-Hodgkin lymphoma
- Jumping translocations of 11q in acute myeloid leukemia and 1q in follicular lymphoma
- Karyotypically independent clones with del(11q) and trisomy 10 in acute myeloid leukemia: trisomy 10 may appear as an additional change
- miR expression in MYC-negative DLBCL/BL with partial trisomy 11 is similar to classical Burkitt lymphoma and different from diffuse large B-cell lymphoma
- Molecular basis of aggressive disease in chronic lymphocytic leukemia patients with 11q deletion and trisomy 12 chromosomal abnormalities
- Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies
- Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication
- Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation
- Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings
- Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation
- Novel translocation t(3;11)(p21;q24) in multiple myeloma characterised by FISH
- Overexpression of the MLL gene combined with 11q trisomy in a child with acute lymphoblastic leukemia
- Partial chromosomal 11q trisomy as an unbalanced result of t(11;13)(q23.1;q34)mat in two sisters
- Partial monosomy 11q and trisomy 12q: variable expression in two siblings
- Partial trisomy 11, dup(11)(q23q13), as a defect characterizing lymphomas with Burkitt pathomorphology without MYC gene rearrangement
- Partial trisomy 11q and partial monosomy 12p due to the maternal translocation (11q;12p)
- Partial trisomy 11q syndrome (11q23.1-->11qter) due to de novo t (11q; 13q) detected by multicolor fluorescence in situ hybridisation
- 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
- Partial trisomy of 11q23.3-q25 inherited from a maternal low-level mosaic unbalanced translocation
- Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature
- Precocious puberty associated with partial trisomy 18q and monosomy 11q
- Predictive role of interphase cytogenetics for survival of patients with multiple myeloma
- Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry
- Prenatal diagnosis of a case with combined Wolf-Hirschhorn syndrome and Jacobsen syndrome
- Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system
- Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly
- Proof of partial imbalances 6q and 11q due to maternal complex balanced translocation analyzed by microdissection of multicolor labeled chromosomes (FISH-MD) in a patient with Dandy-Walker variant
- Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis
- Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11q
- Serum angiogenin is not elevated in patients with early B-cell chronic lymphocytic leukemia but is prognostic factor for disease progression
- Study on clinical and biological characteristics of childhood acute leukemia with MLL gene rearrangements
- Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: molecular characterization of two der(11)t(11;16)
- Subtle familial translocation t(11;22)(q24.2;q13.33) resulting in Jacobsen syndrome and distal trisomy 22q13.3: further details of genotype-phenotype maps
- Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation
- Surface antigen expression in chronic lymphocytic leukemia: clustering analysis, interrelationships and effects of chromosomal abnormalities
- Terminal deletion 6q syndrome with 11q partial trisomy mosaicism due to maternal balanced translocation
- Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects an
- The clinical significance of tumor necrosis factor-alpha plasma level in patients having chronic lymphocytic leukemia
- The influence of different chromosomal aberrations on molecular cytogenetic parameters in chronic lymphocytic leukemia
- Trisomy 11 as an isolated abnormality in acute myeloid leukemia is associated with unfavorable prognosis but not with an NPM1 or KIT mutation
- Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up
- Ultrasound, Echocardiography, MRI, and Genetic Analysis of a Fetus with Congenital Diaphragmatic Hernia and Partial 11q Trisomy
- Unbalanced translocation der(7)t(7q;11q): a new recurrent aberration leading to partial monosomy 7q and trisomy 11q in acute myeloid leukemia
- Upper airway malformation associated with partial trisomy 11q
- V(H) mutation status, CD38 expression level, genomic aberrations, and survival in chronic lymphocytic leukemia
- Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter