Derivative 11;22 (Emanuel) Syndrome: A Case Report and A Review
Small supernumerary marker chromosome - Wikipedia
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 ...
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification | SpringerLink
![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
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
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
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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Marker Chromosome - an overview | ScienceDirect Topics
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
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
A supernumerary bisatellited marker originating from chromosome 22... | Download Scientific Diagram
A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22 | PNAS
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human 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
A) Karyogram of the fetus with supernumerary marker chromosome derived... | Download Scientific Diagram
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | Molecular Cytogenetics | Full Text
Fluorescence In Situ Hybridisation result: the extra marker chromosome... | Download Scientific Diagram
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A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man. - Abstract - Europe PMC
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
