![Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine](https://ijrm.ir/files/site1/images/2021/May/9/Figure_2.jpg)
Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine
![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
![First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | Molecular Cytogenetics | Full Text First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | Molecular Cytogenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13039-022-00601-5/MediaObjects/13039_2022_601_Fig3_HTML.png)
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | 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/F2.large.jpg)
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
![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
![Diagnostics | Free Full-Text | Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray Diagnostics | Free Full-Text | Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray](https://www.mdpi.com/diagnostics/diagnostics-11-01457/article_deploy/html/images/diagnostics-11-01457-g001.png)
Diagnostics | Free Full-Text | Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray
![SciELO - Brasil - Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with SciELO - Brasil - Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with](https://minio.scielo.br/documentstore/1678-4685/Q66rsGzcFD4hMgsdW6rFmGB/c90574752cf775ff51630409893bab360767c013.jpg)
SciELO - Brasil - Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with
![A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype | Semantic Scholar A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/3e33e014aa13f8476835f19f10d79650bec32941/3-Figure2-1.png)
A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype | Semantic Scholar
![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
![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)
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
![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
![Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13039-021-00533-6/MediaObjects/13039_2021_533_Fig1_HTML.png)
Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text
![FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22) | European Journal of Human Genetics FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22) | European Journal of Human Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsj.ejhg.5201378/MediaObjects/41431_2005_Article_BF5201378_Fig1_HTML.jpg)
FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22) | European Journal of Human Genetics
![OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization](http://www.lidsen.com/image/data/20180913/genetics-02-03-03401.jpg)