• 17-18 RING-CHROMOSOMES AND CONGENITAL MALFORMATIONS IN A YOUNG GIRL
• A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome
• A case of ring chromosome 18 syndrome treated with a combined orthodontic-prosthodontic approach
• A Case of Ring Chromosome 18 with Single Umbilical Artery Detected During Prenatal Period
• A case report of Ring chromosome 18 with systemic Lupus Erythematosus and Crohn's disease
• A female with monosomy 18 mosaicism: a previously undescribed chromosome abnormality
• A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome
• A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18
• Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination
• Abnormal corneal epithelial maintenance in mice heterozygous for the micropinna microphthalmia mutation Mp
• Abnormal myelination in a patient with ring chromosome 18
• Abnormal myelination in ring chromosome 18 syndrome
• Adults with Chromosome 18 Abnormalities
• Agammaglobulinaemia in a girl with a mosaic of ring 18 chromosome
• An unexpected finding in a child with neurological problems: mosaic ring chromosome 18
• Analysis of fetal DNA in the maternal venous blood for abnormalities of chromosomes 13, 16, 18 and 21 in first-trimester spontaneous miscarriage
• Anencephaly with holoprosencephalic facies due to ring chromosome 18
• Anesthetic Management of a Patient With Ring 18 Syndrome
• Auto-ubiquitination-induced degradation of MALT1-API2 prevents BCL10 destabilization in t(11;18)(q21;q21)-positive MALT lymphoma
• Autoimmune polyendocrinopathy associated with ring chromosome 18
• Blaschkoid hypermelanosis in a patient with ring 18 chromosome
• Breakpoints and deleted genes identification of ring chromosome 18 in a Chinese girl by whole-genome low-coverage sequencing: a case report study
• Case report of de novo dup(18p)/del(18q) and r(18) mosaicism
• Central and peripheral dysmyelination in a 3-year-old girl with ring chromosome 18
• Centromeric association of a microchromosome Y in two male patients
• Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin
• Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18
• Clinical course of a 20-month-old child diagnosed prenatally with mosaic ring chromosome 18 and monosomy 18
• Coamplification of 12p11 and 12q13 approximately q22 in multiple ring chromosomes in a spindle cell sarcoma resolved by novel multicolor fluorescence in situ hybridization analysis
• Common variants near MC4R are associated with fat mass, weight and risk of obesity
• Complete karyotype discrepancy between placental and fetal cells in a case of ring chromosome 18
• Complex hypodiploidy in acute myeloid leukaemia: a United Kingdom Cancer Cytogenetics Group study
• CRISPR-C: circularization of genes and chromosome by CRISPR in human cells
• Cytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p
• Cytogenetic characterization of ten malignant fibrous histiocytomas
• Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q
• De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems
• Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH
• Detection of premature segregation of centromeres in persons exposed to ionizing radiation
• Distinct molecular features of colorectal carcinoma with signet ring cell component and colorectal carcinoma with mucinous component
• Epilepsy and chromosome 18 abnormalities: A review
• Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11→q21::)/
• Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization
• First familial case of ring chromosome 18 and monosomy 18 mosaicism
• Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes
• Fluorescence in situ hybridization: a rapid analysis to verify chromosome aberrations
• Formation of a familial ring chromosome 18 investigated by SNP-array analysis
• Gain of 11q by an additional ring chromosome 11 and trisomy 18 in CD5-positive intravascular large B-cell lymphoma
• Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18
• Genetic determinants of susceptibility to silver nanoparticle-induced acute lung inflammation in mice
• Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism
• Growth hormone deficiency in a girl with ring 18 chromosome syndrome
• Growth hormone deficiency, hypothyroidism and ring chromosome 18: case report
• Growth hormone neurosecretory dysfunction associated with ring chromosome 18
• Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies
• Humoral deficiency in three paediatric patients with genetic diseases
• Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome
• Identification and molecular characterization of a de novo supernumerary ring chromosome 18 in a patient with Klippel-Trenaunay syndrome
• Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene
• Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene(s) on chromosome 18
• Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
• Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: genotype-phenotype correlations
• Large inverted duplications in the human genome form via a fold-back mechanism
• Linkage analysis of families with bipolar illness and chromosome 18 markers
• Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies
• Meiotic behavior of the sex chromosomes in a 45,X/46,X,r(Y)/46,X,dic r(Y) patient whose semen was assessed by fluorescence in situ hybridization
• Meiotic origin of two ring chromosomes 18 in a girl with developmental delay
• Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing
• Molecular cytogenetic diagnosis of a case with ring chromosome 18 syndrome
• Molecular cytogenetics of bone and soft tissue tumors
• Molecular distinction between true centric fission and pericentric duplication-fission
• Monosomy 18p
• Mos 46,XX,r(18).ish r(18)(18ptel-,18qtel-)/46,XX.ish del(18)(18ptel-): an example for successive ring chromosome formation
• Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report
• Mosaic ring chromosome 18 in a Chinese child with epilepsy: a case report and review of the literature
• Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
• Patchy white matter hyperintensity in ring chromosome 18 syndrome
• Patient with three euchromatic supernumerary marker chromosomes derived from chromosomes 1, 12, and 18: characterization and evaluation of the aberrations
• Prenatal diagnosis and fetopathological findings in a fetus with ring chromosome 18
• Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18
• Prognostic significance of the deleted in colorectal cancer gene protein expression in high-risk resected gastric carcinoma
• Rheumatoid arthritis in an adult patient with mosaic distal 18q-, 18p- and ring chromosome 18
• Ring 18 molecular assessment and clinical consequences
• Ring chromosome 18 abnormality in acute myelogenous leukemia: the clinical dilemma
• Ring chromosome 18 in a child with febrile seizures
• Ring chromosome 18 in a fetus with only facial anomalies
• Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects
• Ring chromosome 18: a case report
• Ring chromosome 18q and jumping translocation 18p in an adult male with hypergonadotrophic hypogonadism
• Selective IgM deficiency in a boy with ring chromosome 18
• Sequential numerical changes of chromosomes 7 and 18 in diffuse-type stomach cancer cell lines: combined comparative genomic hybridization, fluorescence in situ hybridization, and ploidy analyses
• Severe epilepsy in an adult with partial trisomy 18q
• Single-nucleotide polymorphism array-based characterization of ring chromosome 18
• Sphincterplasty for Velopharyngeal Insufficiency in the Child Without a Cleft-Palate: Etiologies and Speech Outcomes
• Thai girl with ring chromosome 18 (46XX, r18)
• The Chromosome 18 Clinical Resource Center
• The role of cytogenetics in the classification of soft tissue tumours
• The translin ring specifically recognizes DNA ends at recombination hot spots in the human genome
• Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18
• Tissue-limited ring chromosome 18 mosaicism as a cause of Pitt-Hopkins syndrome