![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
![Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fsrep17408/MediaObjects/41598_2015_Article_BFsrep17408_Fig1_HTML.jpg)
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports
![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
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
![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)
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
![Karyotype of the patient with Marker chromosome : 47,XY,+mar[3]/46,XY[12] | Download Scientific Diagram Karyotype of the patient with Marker chromosome : 47,XY,+mar[3]/46,XY[12] | Download Scientific Diagram](https://www.researchgate.net/publication/264008326/figure/fig5/AS:646465663795201@1531140833647/Karyotype-of-the-patient-with-Marker-chromosome-47-XY-mar3-46-XY12.png)
Karyotype of the patient with Marker chromosome : 47,XY,+mar[3]/46,XY[12] | Download Scientific Diagram
![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/5705c235-1298-4d03-95c4-2e4e27c1957e/humu23683-gra-0001-m.jpg?trick=1668360850770)
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
![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 pigmentary mosaicism of Ito](http://old.scielo.br/img/revistas/gmb/v39n1//1415-4757-gmb-39-1-35-gf02.jpg)
Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito
![Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child | Journal of Medical Genetics Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/38/12/885/F1.large.jpg)
Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child | Journal of Medical Genetics
![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
![Prenatal chromosomal microarray analysis in 2466 fetuses with ultrasonographic soft markers: a prospective cohort study - American Journal of Obstetrics & Gynecology Prenatal chromosomal microarray analysis in 2466 fetuses with ultrasonographic soft markers: a prospective cohort study - American Journal of Obstetrics & Gynecology](https://www.ajog.org/cms/asset/032643bd-ada3-4856-8390-36a0dbe469e5/gr1.jpg)
Prenatal chromosomal microarray analysis in 2466 fetuses with ultrasonographic soft markers: a prospective cohort study - American Journal of Obstetrics & Gynecology
Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians | SpringerLink
![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
![Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 - ScienceDirect Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1028455917300955-gr1.jpg)
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 - ScienceDirect
![Numerical Abnormalities of Chromosomes Caused by the Electric Charges and Their Implications on Down, Turner, Patau and Other Human Syndromes and Aneuploidies Numerical Abnormalities of Chromosomes Caused by the Electric Charges and Their Implications on Down, Turner, Patau and Other Human Syndromes and Aneuploidies](https://www.longdom.org/articles-images/down-syndrome-marker-chromosome-6-132-g012.png)
Numerical Abnormalities of Chromosomes Caused by the Electric Charges and Their Implications on Down, Turner, Patau and Other Human Syndromes and Aneuploidies
![Chromosome Abnormalities: New Insights into Their Clinical Significance in Cancer: Molecular Therapy - Oncolytics Chromosome Abnormalities: New Insights into Their Clinical Significance in Cancer: Molecular Therapy - Oncolytics](https://www.cell.com/cms/attachment/6f52e7b1-dea8-4374-b586-5742892dfe2f/fx1_lrg.jpg)
Chromosome Abnormalities: New Insights into Their Clinical Significance in Cancer: Molecular Therapy - Oncolytics
![Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13039-016-0273-5/MediaObjects/13039_2016_273_Fig3_HTML.gif)