Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification | SpringerLink
Marker Chromosome - an overview | ScienceDirect Topics
Duane syndrome associated with the Cat Eye syndrome: a case report | Eye
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | Molecular Cytogenetics | Full Text
PDF) FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22) | Oliver Bartsch and Dr. Sasan Rasi - Academia.edu
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22 – topic of research paper in Clinical medicine.
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
Derivative 11;22 (Emanuel) Syndrome: A Case Report and A Review
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome | Journal of Medical Genetics
![PDF] Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/25774276fcfe22a4feef6585edaecefad3f19a00/2-Figure1-1.png "PDF] Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation. | Semantic Scholar")
PDF] Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation. | Semantic Scholar
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
![PDF] Partial Tetrasomy of Chromosome 22q11.1 Resulting from a Supernumerary Isodicentric Marker Chromosome in a Boy with Cat-eye Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ace5d13c0d3a784b5cbf2f820a364120cf287072/3-Figure3-1.png "PDF] Partial Tetrasomy of Chromosome 22q11.1 Resulting from a Supernumerary Isodicentric Marker Chromosome in a Boy with Cat-eye Syndrome | Semantic Scholar")
PDF] Partial Tetrasomy of Chromosome 22q11.1 Resulting from a Supernumerary Isodicentric Marker Chromosome in a Boy with Cat-eye Syndrome | Semantic Scholar
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A) Karyogram of the fetus with supernumerary marker chromosome derived... | Download Scientific Diagram
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
Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report | Molecular Cytogenetics | Full Text
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 non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man. - Abstract - Europe PMC
De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches - Malvestiti - 2014 - Prenatal Diagnosis - Wiley ...
Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrom
