Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature | Journal of Medical Case Reports | Full Text
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features
A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss
Study clarifies link between 15q duplication and autism | Spectrum | Autism Research News
Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians | SpringerLink
A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype | Journal of Medical Genetics
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
Chromosome 15 - Wikipedia
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
Genetics of AS – Angelman Syndrome Foundation
A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype | Journal of Medical Genetics
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
![Karyotyping of subject shows isodicentric chromosome 15 [idic(15)]. (A)... | Download Scientific Diagram](https://www.researchgate.net/publication/236934735/figure/fig2/AS:601682983530507@1520463810217/Karyotyping-of-subject-shows-isodicentric-chromosome-15-idic15-A-Idic15-is.png "Karyotyping of subject shows isodicentric chromosome 15 [idic(15)]. (A)... | Download Scientific Diagram")
Karyotyping of subject shows isodicentric chromosome 15 [idic(15)]. (A)... | Download Scientific Diagram
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
![PDF] Ring Chromosome 15 Syndrome: Case Report and Literature Review | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/83c839482fbafec7fc77c66016ec9ae374e0c48c/3-Figure1-1.png "PDF] Ring Chromosome 15 Syndrome: Case Report and Literature Review | Semantic Scholar")
PDF] Ring Chromosome 15 Syndrome: Case Report and Literature Review | Semantic Scholar
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text
PDF) A patient with Prader-Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomy | Dvorah Abeliovich - Academia.edu
Neurodevelopmental Disorders Associated with Chromosome 15
A patient with a supernumerary marker chromosome (15), Angelman syndrome, and uniparental disomy resulting from paternal meiosis II non-disjunction | Journal of Medical Genetics
IJMS | Free Full-Text | Chromosomal Microarray Study in Prader-Willi Syndrome
Supernumerary Marker of Chromosome 15 Associated with Paternal Uniparental Disomy in a Case with Angelman Syndrome
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
