Male Infertility Associated with a Supernumerary Marker Chromosome
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities | IntechOpen
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,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Figure 2 | Anatomical Asplenia in Cat Eye Syndrome: An Expansion of the Disease Spectrum
The G-banded karyotype. mar = marker chromosome. | Download Scientific Diagram
Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
Genetics
Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito
![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
Marker Chromosome - an overview | ScienceDirect Topics
Small supernumerary marker chromosome - Wikipedia
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
Edwards syndrome - Wikipedia
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities - ScienceDirect
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Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
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Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
