Neocentromere - Wikipedia
Small supernumerary marker chromosome - Wikipedia
![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
Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text
KoreaMed
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
A supernumerary bisatellited marker originating from ch | Open-i
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review - ScienceDirect
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
Identification of satellited markers by microdissection and fluorescence in situ hybridization: a clinical case of isodicentric chromosome 22 | Egyptian Journal of Medical Human Genetics | Full Text
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
Marker Chromosomes | 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
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
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Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
Genetics
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Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
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 unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7
