1. Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report
   H. C. Manju et al, 2022, Molecular Cytogenetics CrossRef
2. Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array
   Lili Zhou et al, 2020, Molecular Cytogenetics CrossRef
3. Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome
   Pascale Kleinfinger et al, 2022, Frontiers in Genetics CrossRef
4. 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, Frontiers in Pediatrics CrossRef
5. Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors
   Ron Hochstenbach et al, 2015, Molecular Syndromology CrossRef
6. 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, Frontiers in Genetics CrossRef
7. Prenatal and Postnatal Clinical Spectrum of a Mosaic Small Supernumerary Marker Chromosome 22
   Esra Tug et al, 2019, International Journal of Pediatrics and Child Health CrossRef
8. Small supernumerary marker chromosomes in prenatal diagnosis—molecular characterization and clinical outcomes
   Ivana Joksic et al, 2024, Frontiers in Genetics CrossRef
9. 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, Cytogenetic and Genome Research CrossRef
10. Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review
    Thomas Liehr et al, 2019, Frontiers in Genetics CrossRef
11. Molecular characterization of supernumerary marker chromosomes found as unexpected chromosome abnormalities in nine prenatal and nine postnatal samples
    Meena Lall et al, 2019, Obstetrics & Gynecology International Journal CrossRef
12. FISH – The Best Technique in Characterization of Prenatally Detected Small Supernumerary Marker Chromosomes (sSMC)
    Frenny J Sheth et al, 2016, International Journal of Pregnancy & Child Birth CrossRef
13. 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
14. Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome
    Si He et al, 2020, Molecular Cytogenetics CrossRef
15. Clinical characteristics and laboratory diagnosis of Pallister-Killian syndrome
    N.V. Shilova et al, 2024, CrossRef
16. Identification of satellited markers by microdissection and fluorescence in situ hybridization: a clinical case of isodicentric chromosome 22
    Natalya A. Lemskaya et al, 2021, Egyptian Journal of Medical Human Genetics CrossRef
17. Three-Year Follow-Up of a Prenatally Ascertained Apparently Non-Mosaic sSMC(10): Delineation of a Non-Critical Region
    Laura Barranco et al, 2015, Cytogenetic and Genome Research CrossRef
18. Small Supernumerary Marker Chromosomes in Human Infertility
    Narjes Armanet et al, 2015, Cytogenetic and Genome Research CrossRef
19. Molecular cytogenetic characteristics of small supernumerary marker chromosomes 15 and 22 in asymptomatic carriers
    DA Yurchenko et al, 2024, Bulletin of Russian State Medical University CrossRef