Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
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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Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
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
The G-banded karyotype. mar = marker chromosome. | Download Scientific Diagram
Small supernumerary marker chromosome - Wikipedia
A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7
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
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
![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
A supernumerary marker chromosome originating from two diVerent regions of chromosome 18
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Mosaic Ring-like Small Supernumerary Marker Chromosome and Gene Mutation in a Male With Intermittent Azoospermia: A Rare Case Report - Jianzhong Zhang, Longyu Li, Qiaoqin Li, Zhonglin Cai, Binbin Wang, Jing Wang,
Male Infertility Associated with a Supernumerary Marker Chromosome
Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine
![PDF] A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/d632adcfaa0b331c8dc50cd81c619c9aea5210fc/2-Figure1-1.png "PDF] A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome. | Semantic Scholar")
PDF] A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome. | Semantic Scholar
A Search for Uniparental Disomy in Carriers of Supernumerary Marker Chromosomes | European Journal of Human Genetics
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Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
Marker Chromosomes | SpringerLink
Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl | Journal of Medical Genetics
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
