![Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes](https://www.mdpi.com/biomedicines/biomedicines-10-01102/article_deploy/html/images/biomedicines-10-01102-g001-550.jpg)
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
![Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping](https://www.spandidos-publications.com/article_images/or/28/2/OR-28-02-0533-g03.jpg)
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping
![Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report](https://www.spandidos-publications.com/article_images/etm/19/4/etm-19-04-2927-g00.jpg)
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
![A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/38/8/559/F5.large.jpg)
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
![The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities | IntechOpen The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities | IntechOpen](https://www.intechopen.com/media/chapter/54502/media/F2.png)
The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities | IntechOpen
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
![Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome - ScienceDirect Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1028455920302990-gr1.jpg)
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome - ScienceDirect
![Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function](https://www.mdpi.com/genes/genes-11-01511/article_deploy/html/images/genes-11-01511-g010.png)
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
![Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/34d7d3ef-676f-41f5-9513-771936783ffe/humu23683-fig-0001-m.jpg)
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
![Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsj.ejhg.5201473/MediaObjects/41431_2005_Article_BF5201473_Fig1_HTML.jpg)
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
![Figure 1.3 from Small supernumerary marker chromosomes (sSMC) : why do they break, where they break and how to distinguish harmful from harmless sSMC? | Semantic Scholar Figure 1.3 from Small supernumerary marker chromosomes (sSMC) : why do they break, where they break and how to distinguish harmful from harmless sSMC? | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/4eb58a4c7f8e4d427466150381c5292ea24bd0e5/19-Figure1.3-1.png)
Figure 1.3 from Small supernumerary marker chromosomes (sSMC) : why do they break, where they break and how to distinguish harmful from harmless sSMC? | Semantic Scholar
![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 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](https://d3i71xaburhd42.cloudfront.net/a76783362b3c45f430a78b20b4b8d18550bf3bd8/3-Figure1-1.png)
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 new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2F1755-8166-1-4/MediaObjects/13039_2007_Article_4_Fig1_HTML.jpg)
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text
![A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/37/2/121/F1.large.jpg)