1. Sequence Composition and Evolution of Mammalian B Chromosomes
    Nikolay Rubtsov et al, 2018, Genes CrossRef
  2. FISH – The Best Technique in Characterization of Prenatally Detected Small Supernumerary Marker Chromosomes (sSMC)
    Frenny J Sheth et al, 2016, IPCB CrossRef
  3. Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review
    Thomas Liehr et al, 2019, Front. Genet. CrossRef
  4. Molecular Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Chromosome Y in an Infertile Male with Apparently Normal Phenotype: A Case Report and Literature Review
    Na An et al, 2019, BioMed Research International CrossRef
  5. Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome
    Si He et al, 2020, Mol Cytogenet CrossRef
  6. Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array
    Lili Zhou et al, 2020, Mol Cytogenet CrossRef
  7. De novo 8p21.3→ p23.3 Duplication With t(4;8)(q35;p21.3) Translocation Associated With Mental Retardation, Autism Spectrum Disorder, and Congenital Heart Defects: Case Report With Literature Review
    Cristina Gug et al, 2020, Front. Pediatr. CrossRef
  8. Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
    Tatyana V. Karamysheva et al, 2020, Genes CrossRef
  9. Identification of satellited markers by microdissection and fluorescence in situ hybridization: a clinical case of isodicentric chromosome 22
    Natalya A. Lemskaya et al, 2021, Egypt J Med Hum Genet CrossRef
  10. Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray
    Tien-Yu Yao et al, 2021, Diagnostics CrossRef
  11. Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report
    H. C. Manju et al, 2022, Mol Cytogenet CrossRef
  12. Meiotic Segregation of an Isodicentric Derived from Chromosome 15 in Sperm of a Patient with Mosaic Karyotype: Case Report and Review of the Literature
    Sahar El Fekih et al, 2022, Cytogenet Genome Res CrossRef
  13. Small Supernumerary Marker Chromosomes in Human Infertility
    Narjes Armanet et al, 2015, Cytogenet Genome Res CrossRef
  14. Three-Year Follow-Up of a Prenatally Ascertained Apparently Non-Mosaic sSMC(10): Delineation of a Non-Critical Region
    Laura Barranco et al, 2015, Cytogenet Genome Res CrossRef
  15. Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors
    Ron Hochstenbach et al, 2015, Mol Syndromol CrossRef
  16. Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome
    Pascale Kleinfinger et al, 2022, Front. Genet. CrossRef
  17. Prenatal and Postnatal Clinical Spectrum of a Mosaic Small Supernumerary Marker Chromosome 22
    Esra Tug et al, 2019, Int. J. Pediatr. Child Health CrossRef
  18. Small supernumerary marker chromosomes in prenatal diagnosis—molecular characterization and clinical outcomes
    Ivana Joksic et al, 2024, Front. Genet. CrossRef
  19. Molecular cytogenetic characteristics of small supernumerary marker chromosomes 15 and 22 in asymptomatic carriers
    DA Yurchenko et al, 2024, BRSMU CrossRef
  20. A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature
    Fatima Ouboukss et al, 2024, Front. Genet. CrossRef
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    N.V. Shilova et al, 2024 CrossRef