• A case of de novo partial tetrasomy of distal 6p and review of the literature
• A case of partial trisomy of chromosome 8p associated with autism
• A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report
• A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones
• Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization
• An early, nonrandom karyotypic change in immortal Syrian hamster cell lines transformed by asbestos: trisomy of chromosome 11
• Analysis of Chromosome 3, 7 and 8 Centromeric Regions in Bronchial Lavage Specimens by FISH
• Aneusomy of chromosomes 7, 8, and 17 and amplification of HER-2/neu and epidermal growth factor receptor in Gleason score 7 prostate carcinoma: a differential fluorescent in situ hybridization study of Gleason pattern 3 and 4 using tissue microarray
• Application of personal computer to an analysis of small de novo chromosomal insertion: a case of de novo 3q2 trisomy with ins(8;3)
• Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy
• Centromere-telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy
• Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations
• Chromosome 8 : complete trisomy and segmental trisomies
• Chromosome abnormalities in colorectal adenomas: two cytogenetic subgroups characterized by deletion of 1p and numerical aberrations
• Chromosome analysis of renal cell carcinoma
• Chronic lymphocytic leukemia with a novel der(8;15)(q10;q10) translocation
• Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p
• Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report
• Clonal evolution and clinical significance of trisomy 8 in acquired bone marrow failure
• Complete and partial trisomy of different segments of chromosome 8: case reports and review
• Congenital heart disease in partial trisomy 8p with special reference to pulmonary hypertension in two siblings
• Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation
• Cytogenetic profile predicts prognosis of patients with clear cell renal cell carcinoma
• De novo case of a partial trisomy 4p and a partial monosomy 8p
• Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case
• Duplication of 8p with minimal phenotypic effect transmitted from a mother to her two daughters
• Establishment and validation of prognostic nomogram in acute leukemia with trisomy 8
• Familial complex chromosome rearrangement giving rise to balanced and unbalanced recombination products
• Familial partial trisomy 8p without dysmorphic features and only mild mental retardation
• Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development
• Genetic characterization of immortalized human prostate epithelial cell cultures. Evidence for structural rearrangements of chromosome 8 and i(8q) chromosome formation in primary tumor-derived cells
• Genotype-phenotype association studies of chromosome 8p inverted duplication deletion syndrome
• High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8
• Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8
• Inv dup (8) (p21.1----22.1): further case report and a new hypothesis on the origin of the chromosome abnormality
• Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses
• Inverted duplication of 8p: ten new patients and review of the literature
• Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q
• Isochromosome 8q formation is associated with 8p loss of heterozygosity in a prostate cancer cell line
• Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome
• Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter)
• Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication
• Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter
• Molecular genetic and clinical characterization of acute myeloid leukemia with trisomy 8 as the sole chromosome abnormality
• Mosaic "tetrasomy" 8p: case report and review of the literature
• Mosaic tetrasomy 8p in two patients: clinical data and review of the literature
• Mosaicism for an ectopic NOR at 8pter and a complex rearrangement of chromosome 8 in a patient with severe psychomotor retardation
• Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosum
• Normal adaptive function with learning disability in duplication 8p including band p22
• Oculoauriculovertebral spectrum phenotype caused by an unbalanced t(5;8)(p15.31;p23.1) rearrangement
• Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood
• Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization
• Partial monosomy 8p and partial trisomy 8p with moderate mental retardation
• Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
• Partial monosomy 8p/trisomy 8q in a newborn infant due to a maternal three-way translocation: Clinical and cytogenetic comparison with San Luis Valley syndrome
• Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literature
• Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report
• Partial trisomy and monosomy 8p due to inversion duplication
• Partial Trisomy of Chromosome 13 with a Novel Translocation (8 ; 13) and Unique Clinical Presentation in a Palestinian Infant
• Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization
• Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family
• Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats
• Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques
• Prenatal diagnosis of 18p deletion and 8p trisomy syndrome: literature review and report of a novel case
• Prenatal diagnosis of a fetus with partial trisomy 8p resulting from a balanced maternal translocation by array-based comparative genomic hybridization
• Prenatal diagnosis of a partial 8p trisomy
• Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart
• Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes
• Prenatal diagnosis of inverted duplication deletion 8p syndrome mimicking trisomy 18
• Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal
• Prognosis of secondary acute myeloid leukemia is affected by the type of the preceding hematologic disorders and the presence of trisomy 8
• Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome
• San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease
• Secondary trisomy or mosaic "tetrasomy" 8p
• The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology
• Three-year-old girl with partial trisomy 4p and partial monosomy 8p with resemblance to Brachmann-de Lange syndrome--another locus for Brachmann-de Lange syndrome on 4p?
• Topographical analysis of telomere length and correlation with genomic instability in whole mount prostatectomies
• Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype
• Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study
• Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum development
• Trisomy 8p and Rieger malformation
• Trisomy 8p by malsegregation of a t(5;8)(p15;p11)mat in a case of XY pure gonadal dysgenesis
• Trisomy 8p due to the 3:1 segregation of the balanced translocation t(8;15)mat
• Trisomy 8p: unusual origin detected by fluorescence in situ hybridization
• Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature
• Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3)
• Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities
• Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8p
• Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion