A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
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 of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine
G-banded karyotype showing the marker chromosome. | Download Scientific Diagram
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
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Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
![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
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 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
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
Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia - ScienceDirect
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping
Genetics
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | Molecular Cytogenetics | Full Text
Small supernumerary marker chromosome - Wikipedia
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
