A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22 | PNAS
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
Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report | Molecular Cytogenetics | Full Text
Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives | SpringerLink
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Marker Chromosome - an overview | ScienceDirect Topics
Derivative 11;22 (Emanuel) Syndrome: A Case Report and A Review
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
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
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 ...
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification | SpringerLink
Duane syndrome associated with the Cat Eye syndrome: a case report | Eye
A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man. - Abstract - Europe PMC
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 of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
FISH (Genetics)
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.
Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text
TL
A supernumerary bisatellited marker originating from chromosome 22... | Download Scientific Diagram
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
A) Karyogram of the fetus with supernumerary marker chromosome derived... | Download Scientific Diagram
Representation of Chromosome 22 with enlargement of the 22q11.2 region... | Download Scientific Diagram
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![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
![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")