Small supernumerary marker chromosome - Wikipedia
Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature | Molecular Cytogenetics | Full Text
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
Targeting chromosome trisomy for chromosome editing | Scientific Reports
Marker Chromosomes | SpringerLink
Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array | Molecular Cytogenetics | Full Text
Marker Chromosomes | SpringerLink
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports
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
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
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
An extra marker chromosome in karyotype | Download Scientific Diagram
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text
Figure 1 from Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito | Semantic Scholar
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review - ScienceDirect
![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")
Karyotype of the patient with Marker chromosome : 47,XY,+mar[3]/46,XY[12] | Download Scientific Diagram
Chromosome 2 from the new NCCCWA linkage map is shown as an example.... | Download Scientific Diagram
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
