Neocentromere - Wikipedia
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
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | Molecular Cytogenetics | Full Text
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text
The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities | IntechOpen
A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
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A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
SciELO - Brasil - 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
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
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A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping
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
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3 - ScienceDirect
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
Marker Chromosomes | SpringerLink
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
Marker Chromosome - an overview | ScienceDirect Topics
