• A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux
• A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss
• A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy
• A human gene coding for a membrane-associated nucleic acid-binding protein
• A new case of ring chromosome 9
• A new case of ring chromosome 9
• A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease
• A patient with ring 9 chromosome 46,XY,r(9)(p24.1q34.3)
• A ring chromosome 9 in an infant with malformations
• 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 with t(6;9) (p23;q34): association with myelodysplasia, basophilia, and initial CD34 negative immunophenotype
• Additional chromosomal abnormalities to Ph during the clinical course in patients with acute lymphoblastic leukemia
• Analysis of genetics mechanism for the phenotypic diversity in a patient carrying a rare ring chromosome 9
• Analysis of ring chromosome 9 syndrome with fluorescence in situ hybridization
• Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder
• Another case of ring chromosome 9 associated with gastroesophageal reflux
• Apparent Prader-Willi phenotype in a woman with ring chromosome 9
• Azoospermia and ring chromosome 9--a case report
• C-band morphology of T(8;9)/8;9 in Blattella germanica
• Characterisation of the rhoph2 gene of Plasmodium falciparum and Plasmodium yoelii
• Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and FISH analysis
• Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH)
• Chromosomal introgressions from Oryza meridionalis into domesticated rice Oryza sativa result in iron tolerance
• Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases
• Chromosome banding in Amphibia. XXI. Inversion polymorphism and multiple nucleolus organizer regions in Agalychnis callidryas (Anura, Hylidae)
• Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndrome
• Cloning and characterization of LUN, a novel ring finger protein that is highly expressed in lung and specifically binds to a palindromic sequence
• 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
• Concomitant and successive amplifications of MYC in APL-like leukemia
• Congenital hypothyroidism: the Riyadh Military Hospital experience
• Contribution of fluorescence in situ hybridization analyses to the characterization of masked and complex Philadelphia chromosome translocations in chronic myelocytic leukemia
• Cytogenetic findings in a new case of adenoid cystic carcinoma arising in sphenoidal sinus
• Dermatofibrosarcoma protuberans harboring t(9;22)(q32;q12.2)
• Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy
• Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9
• Effect of met-enkephalin on chromosomal aberrations in the lymphocytes of the peripheral blood of patients with multiple sclerosis
• Establishment and characterization of a novel CD34-positive human myeloid leukemia cell line: MHH225 growing in serum-free culture
• Evolutionary and clinical neocentromeres: two faces of the same coin?
• Frequent loss of 9p21 (p16(INK4A)) and other genomic imbalances in human malignant fibrous histiocytoma
• Genome-wide associations of human gut microbiome variation and implications for causal inference analyses
• Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways
• Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome
• Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success
• Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene
• Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations
• Interstitial deletion of chromosome 9q with coexistence of the deleted segment as a ring chromosome. A case report
• Kleefstra syndrome 1 and ring chromosome 9 in a case
• Loss of <em>DMRT1</em> gene in a Mos 45,XY,-9[8]/46,XY,r(9)[29]/47,XY,+idic r(9)× 2[1]/46,XY,idic r(9)[1]/46,XY[1] female presenting with short stature
• Mapping QTLs for horizontal resistance to sheath blight in an elite rice restorer line, Minghui 63
• Mental retardation and congenital malformations associated with a ring chromosome 9
• Metacarpophalangeal pattern profile analysis in a patient with ring (9)/del(9p) mosaicism
• Moderate mental retardation and nonspecific dysmorphic syndrome associated with ring chromosome 9
• Murine NFX.1: isolation and characterization of its messenger RNA, mapping of its chromosomal location and assessment of its developmental expression
• Myelodysplastic syndrome in children: differentiation from acute myeloid leukemia with a low blast count
• Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL
• Phenotypic variability in the chromosome 9 ring
• Physical and functional interaction of Rnf2 with Af9 regulates basal and aldosterone-stimulated transcription of the α-ENaC gene in a renal collecting duct cell line
• Post-mortem studies on two patients with 1-2 band cytogenetic deletions: 10q26----qter and r(9)(p24q34)
• Prenatal diagnosis of a female fetus with ring chromosome 9, 46,XX,r(9)(p24q34), and a de novo interstitial 9p deletion
• Prenatal diagnosis of mosaic ring chromosome 9
• Recurrent isochromosome 21 and multiple abnormalities in a patient suspected of having acute myeloid leukemia with eosinophilic differentiation -- a rare case from South India
• Revaluation twenty-three years later of a supernumerary derivative chromosome 9
• Ring chromosome 9
• Ring chromosome 9 [r(9)(p24q34)]: a report of two cases
• Ring Chromosome 9 and Chromosome 9p Deletion Syndrome in a Patient Associated with Developmental Delay: A Case Report and Review of the Literature
• Ring chromosome 9 in a dysmorphic child
• Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literature
• Ring chromosome 9 in a newborn
• Ring chromosome 9 in a newborn male presenting with facial dysmorphia, hypospadias and skeletal abnormalities
• Ring chromosome 9 with a 9p22.3-p24.3 duplication
• Ring chromosome 9: an atypical case
• Ring chromosome 9: identification of a new case by G- and C-banding
• Ring chromosome 9. 46,XY,r(9) in a male with ambiguous external genitalia
• Ring chromosome 9. Case report and review of the literature
• Ring chromosome derived from BCR/ABL in an acute lymphocytic leukemia
• Ring chromosome formation by intra-strand repairing of subtelomeric double stand breaks and clinico-cytogenomic correlations for ring chromosome 9
• Ring finger protein 38 promote non-small cell lung cancer progression by endowing cell EMT phenotype
• Rings and double minutes in a case with blastic phase of chronic myelocytic leukemia
• Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16
• Specific expression and export of the Plasmodium falciparum Gametocyte EXported Protein-5 marks the gametocyte ring stage
• Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas
• Synthetic peptides from conserved regions of the Plasmodium falciparum early transcribed membrane and ring exported proteins bind specifically to red blood cell proteins
• Systems genetics reveals a transcriptional network associated with susceptibility in the maize-grey leaf spot pathosystem
• Targeted mutagenesis of the ring-exported protein-1 of Plasmodium falciparum disrupts the architecture of Maurer's cleft organelles
• The Plasmodium falciparum clag9 gene encodes a rhoptry protein that is transferred to the host erythrocyte upon invasion
• The selection and use of sorghum (Sorghum propinquum) bacterial artificial chromosomes as cytogenetic FISH probes for maize (Zea mays L.)
• TP53, p14ARF, p16INK4a and H-ras gene molecular analysis in intestinal-type adenocarcinoma of the nasal cavity and paranasal sinuses
• Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm
• Unstable mutants of bronze induced by pre-meiotic X-ray treatment in maize
• Variability among Cucurbitaceae species (melon, cucumber and watermelon) in a genomic region containing a cluster of NBS-LRR genes
• Variant intra philadelphia translocation with rearrangement of BCR-ABL and ABL-BCR within the same chromosome in a patient with cALL