Male Infertility Associated with a Supernumerary Marker Chromosome
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
Small supernumerary marker chromosome - Wikipedia
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
Marker Chromosomes | SpringerLink
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | 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
A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
The G-banded karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
G-banded karyotype showing the marker chromosome. | Download Scientific Diagram
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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
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
![PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0653e5cd80daeba739f8717a277fed33064ad223/3-Figure1-1.png "PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic Scholar")
PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic Scholar
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 of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine
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
![PDF] Molecular Cytogenetic Characterization of Supernumerary Marker Chromosomes by Chromosomal Microarray | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0fa45e52621b60f1144370d98f1ffcd6f6f0f2e4/3-Figure1-1.png "PDF] Molecular Cytogenetic Characterization of Supernumerary Marker Chromosomes by Chromosomal Microarray | Semantic Scholar")
PDF] Molecular Cytogenetic Characterization of Supernumerary Marker Chromosomes by Chromosomal Microarray | Semantic Scholar
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
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 karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
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
