• "Double-hit" chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain
• 17p Deletion in acute myeloid leukemia and myelodysplastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ
• A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samples
• A brief commentary on "Refractory anemia with ring sideroblasts associated with i(17q) and mutation of the TP53 gene"
• A case of dermatofibrosarcoma protuberans of the vulva with a COL1A1/PDGFB fusion identical to a case of giant cell fibroblastoma
• A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17
• A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families
• A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15
• A novel aberration of COL1A1-PDGFB fusion as an insertion in chromosome 15 in one case of dermatofibrosarcoma protuberans involving a rare location
• A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15
• A UK NEQAS ISH multicenter ring study using the Ventana HER2 dual-color ISH assay
• Acute leukemia with t(1;3)(p36;q21), evolution to t(1;3)(p36;q21), t(14;17)(q32;q21), and loss of red cell A and Le(b) antigens
• Acute myeloid leukemia and myelodysplasia following intensive chemotherapy for breast cancer
• Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder
• Assignment of the human homologue of the mTRiC-P5 gene (TRIC5) to band 1q23 by fluorescence in situ hybridization
• Association between acute promyelocytic leukemia and ring chromosome 6
• Association of HER-2 copy number and HER-2/CEP-17 ratio with neoadjuvant taxane-containing chemotherapy sensitivity in locally advanced breast cancer
• BRCA1 protein level is not affected by peptide growth factors in MCF10A cell line
• cDNA cloning of a human brain finger protein, BFP/ZNF179, a member of the RING finger protein family
• Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells
• CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature
• Characterisation of the PML/RAR alpha rearrangement associated with t(15;17) acute promyelocytic leukaemia
• Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1)
• Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia
• Chromosome 17
• Chromosome 17 copy numbers and incidence of p 53 gene deletion in gastric cancer cells. Dual color fluorescence in situ hybridization analysis
• Chromosome mapping of human (ZNF147) and mouse genes for estrogen-responsive finger protein (efp), a member of the RING finger family
• Cloning, genomic structure, and expression of mouse ring finger protein gene Znf179
• COL1A1-PDGFB fusion in a pediatric Bednar tumor with 2 copies of a der(22)t(17;22)
• COL1A1-PDGFB fusion in a ring chromosome 4 found in a dermatofibrosarcoma protuberans
• Complex and segmental uniparental disomy updated
• Complex hypodiploidy in acute myeloid leukaemia: a United Kingdom Cancer Cytogenetics Group study
• Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans
• Constitutional ring chromosomes and tumour suppressor genes
• Data on the effects of <em>Hyptis</em> spp. and <em>Lycium</em> spp. plant extracts in <em>C. elegans</em> models of genetically determined neurodegenerative diseases
• Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma
• Dermatofibrosarcoma protuberans
• Detection of COL1A1-PDGFB fusion transcripts in dermatofibrosarcoma protuberans by reverse transcription-polymerase chain reaction using archival formalin-fixed, paraffin-embedded tissues
• Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes
• Fish analysis of supernumerary ring chromosome in dermatofibrosarcoma protuberans
• Five SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin (SMARC) genes are dispersed in the human genome
• Flecked retina associated with café au lait spots, microcephaly, epilepsy, short stature, and ring 17 chromosome
• Flecked retina associated with ring 17 chromosome
• From cytogenetics to cytogenomics of dermatofibrosarcoma protuberans family of tumors
• Fusion of COL1A1 exon 29 with PDGFB exon 2 in a der(22)t(17;22) in a pediatric giant cell fibroblastoma with a pigmented Bednar tumor component. Evidence for age-related chromosomal pattern in dermatofibrosarcoma protuberans and related tumors
• Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism
• Genetic factors in lissencephaly syndromes: a review
• Genetic instability in pancreatic cancer and poorly differentiated type of gastric cancer
• Genomic and transcriptomic features of dermatofibrosarcoma protuberans: Unusual chromosomal origin of the COL1A1-PDGFB fusion gene and synergistic effects of amplified regions in tumor development
• GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma
• HER2/CEP17 ratio and HER2 immunohistochemistry predict clinical outcome after first-line trastuzumab plus taxane chemotherapy in patients with HER2 fluorescence in situ hybridization-positive metastatic breast cancer
• Heterozygous deletion of chromosome 17p renders prostate cancer vulnerable to inhibition of RNA polymerase II
• Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag
• Hypoventilation in REM sleep in a case of 17p11.2 deletion (Smith-Magenis syndrome)
• Identification of a supernumerary marker derived from chromosome 17 using FISH
• Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene
• Involvement of chromosomes 17 and 22 in dermatofibrosarcoma protuberans
• Isolation of the mouse homologue of BRCA1 and genetic mapping to mouse chromosome 11
• Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy
• Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17
• Methylation of O6-methylguanine DNA methyltransferase and loss of heterozygosity on 19q and/or 17p are overlapping features of secondary glioblastomas with prolonged survival
• Microsatellite instability in young patients with colorectal cancer
• Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints location
• Miller-Dieker syndrome with ring chromosome 17
• Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism
• Molecular genetics of dermatofibrosarcoma protuberans: an update
• Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation
• Potentially important microRNA cluster on chromosome 17p13.1 in primary peritoneal carcinoma
• Pre-B acute lymphoblastic leukemia in a 3-year-old boy with pre-acute myelogenous leukemia myelodysplastic syndrome: cytogenetic evidence of common early progenitor cell ontogeny
• Real-world experience with cannabidiol as add-on treatment in drug-resistant epilepsy
• Recurrent isochromosome 21 and multiple abnormalities in a patient suspected of having acute myeloid leukemia with eosinophilic differentiation -- a rare case from South India
• Response of malignant scalp dermatofibrosarcoma to presurgical targeted growth factor inhibition
• Ring 17 syndrome: first clinical report without intellectual disability
• Ring 22 chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences
• Ring Chromosome 10 in a Case of Acute Promyelocytic Leukemia
• Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome
• Ring Chromosome 17 Not Involving the Miller-Dieker Region: A Case with Drug-Resistant Epilepsy
• Ring chromosome 17 syndrome with monosomy 17 mosaicism: case report and literature review
• Ring chromosome 17: phenotype variation by deletion size
• Ring chromosome 17. Case report and review of the literature
• Ring chromosomes in dermatofibrosarcoma protuberans are composed of interspersed sequences from chromosomes 17 and 22
• Ring chromosomes in dermatofibrosarcoma protuberans contain chromosome 17 sequences: fluorescence in situ hybridization
• Ring marker containing 17q and chromosome 22 in a case of dermatofibrosarcoma protuberans
• Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas
• Spectral karyotyping reveals 17;22 fusions in a cytogenetically atypical dermatofibrosarcoma protuberans with a large marker chromosome as a sole abnormality
• Sperizin is a murine RING zinc-finger protein specifically expressed in Haploid germ cells
• Structural and functional analysis of a chimeric protein COL1A1-PDGFB generated by the translocation t(17;22)(q22;q13.1) in Dermatofibrosarcoma protuberans (DP)
• Supernumerary ring chromosome 17 identified by fluorescent in situ hybridization
• Supernumerary ring chromosome in a Bednar tumor (pigmented dermatofibrosarcoma protuberans) is composed of interspersed sequences from chromosomes 17 and 22: a fluorescence in situ hybridization and comparative genomic hybridization analysis
• Supernumerary ring chromosomes containing chromosome 17 sequences. A specific feature of dermatofibrosarcoma protuberans?
• Supernumerary ring chromosomes in dermatofibrosarcoma protuberans may contain sequences from 8q11.2-qter and 17q21-qter: a combined cytogenetic and comparative genomic hybridization study
• Synaptonemal complex analysis in a boar with tertiary, trisomy, product of a rcp(7;17)(q26;q11) translocation
• Telomere shortening and telomere position effect in mild ring 17 syndrome
• The brain finger protein gene (ZNF179), a member of the RING finger family, maps within the Smith-Magenis syndrome region at 17p11.2
• The t(15;17) translocation in acute promyelocytic leukemia
• The ubiquitin-proteasome system and chromosome 17 in cerebellar granule cells and medulloblastoma subgroups
• TP53, p14ARF, p16INK4a and H-ras gene molecular analysis in intestinal-type adenocarcinoma of the nasal cavity and paranasal sinuses
• Transformed dermatofibrosarcoma protuberans: real time polymerase chain reaction detection of COL1A1-PDGFB fusion transcripts in sarcomatous areas
• Translocation, t(17;22)(q22;q13), in dermatofibrosarcoma protuberans: a new tumor-associated chromosome rearrangement
• Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. Dermatofibrosarcoma protuberans and giant cell fibroblastoma