De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference5 articles.
1. A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker (22) chromosomes;Crolla;Am. J. Med. Genet.,1997
2. Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation;Liehr;Cytogenet. Genome Res.,2006
3. Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC;Liehr;Am. J. Med. Genet. A,2006
4. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances;Melo;J. Appl. Genet.,2011
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1. Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array;Molecular Cytogenetics;2023-07-03
2. Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array;Molecular Cytogenetics;2020-05-27
3. Molecular Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Chromosome Y in an Infertile Male with Apparently Normal Phenotype: A Case Report and Literature Review;BioMed Research International;2019-11-19
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