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Ring chromosomes: from formation to clinical potential

https://doi.org/10.1007/s00709-017-1165-1

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1096-8628(19970905)71:4<426::aid-ajmg10>3.0.co;2-iopenalex-snapshot

A case with mosaic di-, tetra-, and octacentric ring Y chromosomes

inferredcites →https://doi.org/10.1002/(sici)1098-2264(199910)26:2<125::aid-gcc4>3.0.co;2-aopenalex-snapshot

A high frequency of tumors with rearrangements of genes of the HMGI(Y) family in a series of 191 pulmonary chondroid hamartomas

inferredcites →https://doi.org/10.1002/1096-8628(20010722)102:1<86::aid-ajmg1390>3.0.co;2-topenalex-snapshot

Mosaic inv dup(8p) marker chromosome with stable neocentromere suggests neocentromerization is a post-zygotic event

inferredcites →https://doi.org/10.1002/ajmg.1320280125openalex-snapshot

Decreased cell viability of fibroblasts from two patients with a ring chromosome: An in vitro reflection of growth failure?

inferredcites →https://doi.org/10.1002/ajmg.1320300406openalex-snapshot

Ring chromosome 11 and café‐au‐lait spots

inferredcites →https://doi.org/10.1002/ajmg.1320560221openalex-snapshot

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization

inferredcites →https://doi.org/10.1002/ajmg.1320570403openalex-snapshot

Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia

inferredcites →https://doi.org/10.1002/ajmg.a.20184openalex-snapshot

Molecular characterization of an inherited ring (19) demonstrating ring opening

inferredcites →https://doi.org/10.1002/ajmg.a.20225openalex-snapshot

Characterization of a supernumerary ring chromosome 1 mosaicism in two cell systems by molecular cytogenetic techniques and review of the literature

inferredcites →https://doi.org/10.1002/ajmg.a.30370openalex-snapshot

Somatic mosaicism of chromosome 7 in a highly proliferating melanocytic congenital naevus in a ring chromosome 7 patient

inferredcites →https://doi.org/10.1002/ajmg.c.31530openalex-snapshot

Chromosome therapy: Potential strategies for the correction of severe chromosome aberrations

inferredcites →https://doi.org/10.1007/bf00200912openalex-snapshot

Inherited ring chromosomes: an analysis of published cases

inferredcites →https://doi.org/10.1007/bf00329128openalex-snapshot

A case of r(21) with stigmata of atypical Down syndrome

inferredcites →https://doi.org/10.1007/bf00401230openalex-snapshot

Ring chromosome 21 in healthy persons: different consequencies in females and in males

inferredcites →https://doi.org/10.1007/bf00446625openalex-snapshot

Analysis of the frequency and distribution of sister chromatid exchanges in cultured human lymphocytes

inferredcites →https://doi.org/10.1007/bf00591082openalex-snapshot

Does ?ring syndrome? exist? An analysis of 207 case reports on patients with a ring autosome

inferredcites →https://doi.org/10.1007/bf02869757openalex-snapshot

The cytogenetics of maize

inferredcites →https://doi.org/10.1007/s00204-016-1766-zopenalex-snapshot

Follow-up studies on genome damage in children after Chernobyl nuclear power plant accident

inferredcites →https://doi.org/10.1007/s00412-016-0621-6openalex-snapshot

A novel system for correcting large-scale chromosomal aberrations: ring chromosome correction via reprogramming into induced pluripotent stem cell (iPSC)

inferredcites →https://doi.org/10.1007/s00431-007-0568-yopenalex-snapshot

An unexpected finding in a child with neurological problems: mosaic ring chromosome 18

inferredcites →https://doi.org/10.1007/s004390050665openalex-snapshot

Increased rate of nondisjunction in sex cells derived from low-quality semen

inferredcites →https://doi.org/10.1007/s004390050960openalex-snapshot

The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells

inferredcites →https://doi.org/10.1007/s10815-014-0388-8openalex-snapshot

Azoospermia and ring chromosome 9—a case report

inferredcites →https://doi.org/10.1007/s13353-015-0311-8openalex-snapshot

Position effect modifying gene expression in a patient with ring chromosome 14

inferredcites →https://doi.org/10.1016/0165-4608(87)90114-2openalex-snapshot

Marker ring chromosome—A new cytogenetic abnormality characterizing lipogenic tumors?

inferredcites →https://doi.org/10.1016/0531-5565(95)02025-xopenalex-snapshot

From telomere loss to p53 induction and activation of a DNA-damage pathway at senescence: The telomere loss/DNA damage model of cell aging

inferredcites →https://doi.org/10.1016/j.ajhg.2007.10.013openalex-snapshot

Mechanisms and Consequences of Small Supernumerary Marker Chromosomes: From Barbara McClintock to Modern Genetic-Counseling Issues

inferredcites →https://doi.org/10.1016/j.arr.2016.05.009openalex-snapshot

Telomere-associated aging disorders

inferredcites →https://doi.org/10.1016/j.cub.2014.08.032openalex-snapshot

Neocentromeres

inferredcites →https://doi.org/10.1016/j.ejmg.2006.11.001openalex-snapshot

Five cases of supernumerary small ring chromosomes 1: Heterogeneity and genotype–phenotype correlation

inferredcites →https://doi.org/10.1016/j.ejmg.2010.09.014openalex-snapshot

Ring chromosome 12 with inverted microduplication of 12p13.3 involving the Von Willebrand Factor gene associated with cryptogenic stroke in a young adult male

inferredcites →https://doi.org/10.1016/j.ejmg.2010.11.015openalex-snapshot

Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report

inferredcites →https://doi.org/10.1016/j.ejmg.2012.02.004openalex-snapshot

Ring chromosome 20

inferredcites →https://doi.org/10.1016/j.ejmg.2012.03.009openalex-snapshot

The ring 14 syndrome

inferredcites →https://doi.org/10.1016/j.eplepsyres.2016.10.004openalex-snapshot

Epilepsy in ring chromosome 20 syndrome

inferredcites →https://doi.org/10.1016/j.fertnstert.2005.06.034openalex-snapshot

Mosaic ring Y chromosome in two normal healthy men with azoospermia

inferredcites →https://doi.org/10.1016/j.rbmo.2011.05.013openalex-snapshot

Azoospermia and paternal autosomal ring chromosomes: case report and literature review

inferredcites →https://doi.org/10.1016/j.stem.2010.12.003openalex-snapshot

Dynamic Changes in the Copy Number of Pluripotency and Cell Proliferation Genes in Human ESCs and iPSCs during Reprogramming and Time in Culture

inferredcites →https://doi.org/10.1016/j.yebeh.2012.02.008openalex-snapshot

Ring chromosome 20 syndrome: Electroclinical description of six patients and review of the literature

inferredcites →https://doi.org/10.1016/s0015-0282(02)04931-2openalex-snapshot

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

inferredcites →https://doi.org/10.1016/s0140-6736(66)91803-4openalex-snapshot

CHROMOSOME STUDIES ON TESTICULAR CELLS FROM 50 SUBFERTILE MEN

inferredcites →https://doi.org/10.1016/s0140-6736(86)91609-0openalex-snapshot

OSTEOGENESIS IMPERFECTA IS LINKED TO BOTH TYPE I COLLAGEN STRUCTURAL GENES

inferredcites →https://doi.org/10.1034/j.1399-0004.2002.620511.xopenalex-snapshot

Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences

inferredcites →https://doi.org/10.1038/35066075openalex-snapshot

Chromosome territories, nuclear architecture and gene regulation in mammalian cells

inferredcites →https://doi.org/10.1038/celldisc.2015.22openalex-snapshot

Uniparental disomy of the entire X chromosome in Turner syndrome patient-specific induced pluripotent stem cells

inferredcites →https://doi.org/10.1038/nature12923openalex-snapshot

Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells

inferredcites →https://doi.org/10.1038/ng0595-117openalex-snapshot

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2

inferredcites →https://doi.org/10.1038/sj.ejhg.5201807openalex-snapshot

Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion

inferredcites →https://doi.org/10.1038/sj.onc.1205566openalex-snapshot

Chromosome instability in human lung cancers: possible underlying mechanisms and potential consequences in the pathogenesis

inferredcites →https://doi.org/10.1073/pnas.12.3.180openalex-snapshot

Correlation between Shape and Behavior of a Chromosome

inferredcites →https://doi.org/10.1080/13668250701829829openalex-snapshot

Ring chromosome 7 in an Indian woman

inferredcites →https://doi.org/10.1083/jcb.139.7.1611openalex-snapshot

Lack of Checkpoint Control at the Metaphase/Anaphase Transition: A Mechanism of Meiotic Nondisjunction in Mammalian Females

inferredcites →https://doi.org/10.1086/342730openalex-snapshot

Neocentromeres: Role in Human Disease, Evolution, and Centromere Study

inferredcites →https://doi.org/10.1091/mbc.e04-03-0207openalex-snapshot

Does a Sentinel or a Subset of Short Telomeres Determine Replicative Senescence?

inferredcites →https://doi.org/10.1093/genetics/23.4.315openalex-snapshot

THE PRODUCTION OF HOMOZYGOUS DEFICIENT TISSUES WITH MUTANT CHARACTERISTICS BY MEANS OF THE ABERRANT MITOTIC BEHAVIOR OF RING-SHAPED CHROMOSOMES

inferredcites →https://doi.org/10.1093/genetics/26.2.234openalex-snapshot

THE STABILITY OF BROKEN ENDS OF CHROMOSOMES IN ZEA MAYS

inferredcites →https://doi.org/10.1093/genetics/77.2.299openalex-snapshot

AN EFFECT OF CENTROMERE FUNCTION ON THE BEHAVIOR OF RING-X CHROMOSOMES IN DROSOPHILA MELANOGASTER

inferredcites →https://doi.org/10.1093/hmg/ddp160openalex-snapshot

Inverted duplications on acentric markers: mechanism of formation

inferredcites →https://doi.org/10.1093/humrep/deh598openalex-snapshot

Mitotic and meiotic behaviour of a naturally transmitted ring Y chromosome: reproductive risk evaluation

inferredcites →https://doi.org/10.1093/nar/gkw422openalex-snapshot

Bromodeoxyuridine does not contribute to sister chromatid exchange events in normal or Bloom syndrome cells

inferredcites →https://doi.org/10.1101/gad.251041.114openalex-snapshot

Telomere position effect: regulation of gene expression with progressive telomere shortening over long distances

inferredcites →https://doi.org/10.1111/j.1399-0004.1975.tb01489.xopenalex-snapshot

The effect of structural aberrations of the chromosomes on reproductive fitness in man

inferredcites →https://doi.org/10.1111/j.1399-0004.1975.tb01490.xopenalex-snapshot

The effect of structural aberrations of the chromosomes on reproductive fitness in man

inferredcites →https://doi.org/10.1111/j.1651-2227.1986.tb10209.xopenalex-snapshot

Severe Growth Failure Associated with Atrophic Intestinal Mucosa and Ring Chromosome 15

inferredcites →https://doi.org/10.1126/science.1225829openalex-snapshot

A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity

inferredcites →https://doi.org/10.1128/mcb.00687-09openalex-snapshot

Safeguarding Entry into Mitosis: the Antephase Checkpoint

inferredcites →https://doi.org/10.1136/jmg.14.3.228openalex-snapshot

Ring chromosome 4.

inferredcites →https://doi.org/10.1136/jmg.17.2.148openalex-snapshot

Ring chromosome 10: 46,XX,r(10)(p15→q26)

inferredcites →https://doi.org/10.1136/jmg.18.3.209openalex-snapshot

Inheritance of a ring 14 chromosome.

inferredcites →https://doi.org/10.1136/jmg.2007.054007openalex-snapshot

Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation

inferredcites →https://doi.org/10.1136/jmg.2008.060442openalex-snapshot

Ring syndrome: still true?

inferredcites →https://doi.org/10.1136/jmg.2008.065052openalex-snapshot

U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements

inferredcites →https://doi.org/10.1136/jmg.2010.080382openalex-snapshot

Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients

inferredcites →https://doi.org/10.1136/jmg.36.12.914openalex-snapshot

Neocentromere formation in a stable ring 1p32-p36.1 chromosome

inferredcites →https://doi.org/10.1155/2016/4645716openalex-snapshot

Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A Case Report and Review of the Literature

inferredcites →https://doi.org/10.1159/000086895openalex-snapshot

Mechanisms of nondisjunction in human spermatogenesis

inferredcites →https://doi.org/10.1159/000138881openalex-snapshot

Ring chromosomes in human neoplasias

inferredcites →https://doi.org/10.1159/000329478openalex-snapshot

Clinical, Cytogenetic and Molecular Study in a Case of r(3) with 3p Deletion and Review of the Literature

inferredcites →https://doi.org/10.1182/blood-2006-10-054247openalex-snapshot

Checkpoint-apoptosis uncoupling in human and mouse embryonic stem cells: a source of karyotpic instability

inferredcites →https://doi.org/10.1186/1471-2350-11-146openalex-snapshot

Genetic investigations on 8 patients affected by ring 20 chromosome syndrome

inferredcites →https://doi.org/10.1186/1471-2350-12-171openalex-snapshot

Mechanisms of ring chromosome formation, ring instability and clinical consequences

inferredcites →https://doi.org/10.1186/1477-7827-2-82openalex-snapshot

The association between male infertility and sperm disomy: evidence for variation in disomy levels among individuals and a correlation between particular semen parameters and disomy of specific chromosome pairs.

inferredcites →https://doi.org/10.1186/1755-8166-2-3openalex-snapshot

Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier

inferredcites →https://doi.org/10.1186/1755-8166-4-5openalex-snapshot

Molecular cytogenetic analysis and clinical manifestations of a case with de novo mosaic ring chromosome 7

inferredcites →https://doi.org/10.1186/1756-8935-7-1openalex-snapshot

Telomere shortening and telomere position effect in mild ring 17 syndrome

inferredcites →https://doi.org/10.1186/s13039-015-0162-3openalex-snapshot

Periventricular heterotopia and white matter abnormalities in a girl with mosaic ring chromosome 6

inferredcites →https://doi.org/10.1212/wnl.0b013e3181bc0158openalex-snapshot

Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures

inferredcites →https://doi.org/10.1371/journal.pbio.2000016openalex-snapshot

Regulation of the Human Telomerase Gene TERT by Telomere Position Effect—Over Long Distances (TPE-OLD): Implications for Aging and Cancer

inferredcites →https://doi.org/10.1371/journal.pgen.1004139openalex-snapshot

Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism

inferredcites →https://doi.org/10.1385/1-59259-828-5:121openalex-snapshot

Analysis of Mammalian Telomere Position Effect

inferredcites →https://doi.org/10.1515/9783112329047openalex-snapshot

Catalogue of Unbalanced Chromosome Aberrations in Man

inferredcites →https://doi.org/10.2478/v10034-011-0049-5openalex-snapshot

Molecular Analysis of Ring Y Chromosome in a 10-Year-Old Boy with Mixed Gonadal Dysgenesis and Growth Hormone Deficiency

inferredcites →https://doi.org/10.3978/j.issn.2224-4336.2015.03.04openalex-snapshot

Autosomal ring chromosomes in human genetic disorders.

inferredcites →https://doi.org/10.4161/cc.4.8.1884openalex-snapshot

Mitotic Instability in Cancer: Is There Method in the Madness?

inferredcites →https://doi.org/10.4161/nucl.36300openalex-snapshot

Chromosome therapy

inferredcites →https://doi.org/10.4238/vol9-1gmr707openalex-snapshot

Ring chromosome instability evaluation in six patients with autosomal rings

inferredcites →https://doi.org/10.7750/biodiscovery.2013.7.1openalex-snapshot

Chromosome rearrangements in sublines of human embryonic stem cell lines hESM01 and hESM03

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4005128openalex-extracted

The Landscape of Extrachromosomal DNA (ecDNA) in the Normal Hematopoiesis and Leukemia Evolution

inferred← citeshttps://doi.org/10.1002/ajmg.a.63925openalex-snapshot

Ring Chromosome 17 Syndrome—A Case Report and Discussion of Diagnostic Methods

inferred← citeshttps://doi.org/10.1007/978-3-031-47530-6_1openalex-snapshot

Historical Perspective of Human Ring Chromosomes

inferred← citeshttps://doi.org/10.1007/978-3-031-47530-6_10openalex-snapshot

Ring Chromosome 6

inferred← citeshttps://doi.org/10.1007/978-3-031-47530-6_15openalex-snapshot

Ring Chromosome 11

inferred← citeshttps://doi.org/10.1007/978-3-031-47530-6_19openalex-snapshot

Ring Chromosome 15

inferred← citeshttps://doi.org/10.1007/978-3-031-47530-6_33openalex-snapshot

Molecular Mechanisms of Ring Chromosome Formation and Instability

inferred← citeshttps://doi.org/10.1007/978-3-031-47530-6_5openalex-snapshot

Ring Chromosome 1

inferred← citeshttps://doi.org/10.1007/s00709-018-1229-xopenalex-snapshot

The genetic self

inferred← citeshttps://doi.org/10.1007/s10577-025-09776-0openalex-snapshot

Sterility and structural variation in an arabidopsis pedigree carrying a ring minichromosome

inferred← citeshttps://doi.org/10.1007/s10803-021-05337-6openalex-snapshot

Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center

inferred← citeshttps://doi.org/10.1016/b978-0-12-820140-4.00003-xopenalex-snapshot

Mosaicism in rare disease

inferred← citeshttps://doi.org/10.1016/j.ajhg.2024.10.006openalex-snapshot

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

inferred← citeshttps://doi.org/10.1016/j.cell.2023.10.015openalex-snapshot

Design, construction, and functional characterization of a tRNA neochromosome in yeast

inferred← citeshttps://doi.org/10.1016/j.coisb.2020.09.001openalex-snapshot

Synthetic yeast genomes for studying chromosomal features

inferred← citeshttps://doi.org/10.1016/j.eplepsyres.2016.10.004openalex-snapshot

Epilepsy in ring chromosome 20 syndrome

inferred← citeshttps://doi.org/10.1016/j.gimo.2025.103475openalex-snapshot

Unravelling ring chromosome structures and formation mechanisms by short-read and long-read genomic sequencing

inferred← citeshttps://doi.org/10.1016/j.htct.2026.108544openalex-snapshot

Karyotypic complexity and mutated TP53 are associated with myeloid neoplasms with ring chromosomes

inferred← citeshttps://doi.org/10.1016/j.jogoh.2026.103164openalex-snapshot

Ring chromosome 6: A case report and literature review

inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.11.015openalex-snapshot

Breaking the vicious circle: Extrachromosomal circular DNA as an emerging player in tumour evolution

inferred← citeshttps://doi.org/10.1038/s41420-022-01189-wopenalex-snapshot

The landscape of extrachromosomal circular DNA (eccDNA) in the normal hematopoiesis and leukemia evolution

inferred← citeshttps://doi.org/10.1038/s41598-021-83399-3openalex-snapshot

Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming

inferred← citeshttps://doi.org/10.1080/19396368.2023.2225682openalex-snapshot

A rare ring chromosome 21 abnormality is associated with azoospermia in two different phenotypically normal cases

inferred← citeshttps://doi.org/10.1080/20905068.2021.1935123openalex-snapshot

Oxidative protein modification and chromosomal instability among type 2 diabetics in Osogbo, Nigeria

inferred← citeshttps://doi.org/10.1093/bbb/zbab215openalex-snapshot

The fission yeast bromodomain protein Bdf2 is required for the growth of cells with circular chromosomes

inferred← citeshttps://doi.org/10.1093/genetics/iyae169openalex-snapshot

Drosophila ring chromosomes interact with sisters and homologs to produce anaphase bridges in mitosis

inferred← citeshttps://doi.org/10.1104/pp.18.00083openalex-snapshot

A Novel Role of Ring Chromosomes as Evolutionary Drivers of Herbicide Resistance

inferred← citeshttps://doi.org/10.1159/000494822openalex-snapshot

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

inferred← citeshttps://doi.org/10.1186/s12920-019-0614-4openalex-snapshot

Clinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review

inferred← citeshttps://doi.org/10.1186/s12935-021-01936-6openalex-snapshot

Small ring has big potential: insights into extrachromosomal DNA in cancer

inferred← citeshttps://doi.org/10.1186/s12935-022-02451-yopenalex-snapshot

Identification of a novel HOOK3-FGFR1 fusion gene involved in activation of the NF-kappaB pathway

inferred← citeshttps://doi.org/10.1186/s13039-018-0372-6openalex-snapshot

Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling

inferred← citeshttps://doi.org/10.1186/s13039-018-0375-3openalex-snapshot

Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22

inferred← citeshttps://doi.org/10.1186/s13039-022-00586-1openalex-snapshot

Growth retardation and congenital heart disease in a boy with a ring chromosome 6 of maternal origin

inferred← citeshttps://doi.org/10.1186/s13039-022-00600-6openalex-snapshot

Mechanisms of structural chromosomal rearrangement formation

inferred← citeshttps://doi.org/10.1186/s13045-020-00960-9openalex-snapshot

Current understanding of extrachromosomal circular DNA in cancer pathogenesis and therapeutic resistance

inferred← citeshttps://doi.org/10.18297/etd/3743openalex-snapshot

Assessing the role of arsenic exposure and MIRNA-186 in skin tumorigenesis and chromosomal instability.

inferred← citeshttps://doi.org/10.2144/fsoa-2019-0024openalex-snapshot

Extrachromosomal Circular DNAs: An Extra Piece of Evidence to Depict Tumor Heterogeneity

inferred← citeshttps://doi.org/10.3389/fgene.2026.1758508openalex-snapshot

Case Report: Prenatal genetic analysis of a rare fetus with 45, X/46, X, dic r (Y; Y)/46, X, r(Y) karyotype

inferred← citeshttps://doi.org/10.3389/fgene.2026.1845616openalex-snapshot

Chromosomal structural abnormalities and tissue-specific mosaicism: insights into false-negative noninvasive prenatal testing

inferred← citeshttps://doi.org/10.3389/fneur.2020.613035openalex-snapshot

Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes

inferred← citeshttps://doi.org/10.3390/biom13020370openalex-snapshot

Exploring Genetic Interactions with Telomere Protection Gene pot1 in Fission Yeast

inferred← citeshttps://doi.org/10.3390/cancers15225439openalex-snapshot

Ring Chromosomes in Hematological Malignancies Are Associated with TP53 Gene Mutations and Characteristic Copy Number Variants

inferred← citeshttps://doi.org/10.3390/genes11121473openalex-snapshot

46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study

inferred← citeshttps://doi.org/10.4172/1747-0862.1000341openalex-snapshot

The Laws of the Ring: Governing Mechanisms, Diagnostic Standards, and Therapeutic Potentials for Human Constitutional Ring Chromosomes

inferred← citeshttps://doi.org/10.47429/lmo.2021.11.2.132openalex-snapshot

A Case of Familial Ring Chromosome 21 Mosaicism

inferred← citeshttps://doi.org/10.5772/intechopen.99812openalex-snapshot

Background, Diagnosis, Types, Management/Prevention and Implications of Chromosomal Abnormalities

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Getting to grips with circular chromosomes

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