A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
![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
Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians | SpringerLink
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review - ScienceDirect
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
FISH with centromere-specific DNA probe D15Z4 (red signals) on a... | Download Scientific Diagram
Study clarifies link between 15q duplication and autism | Spectrum | Autism Research News
Supernumerary Marker of Chromosome 15 Associated with Paternal Uniparental Disomy in a Case with Angelman Syndrome
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature | Journal of Medical Case Reports | Full Text
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text
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
Small supernumerary marker chromosome - Wikipedia
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 supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype | Journal of Medical Genetics
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
Frontiers | Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches
Epigenetic Interface of Autism Spectrum Disorders (ASDs): Implications of Chromosome 15q11–q13 Segment | ACS Chemical Neuroscience
Karyotype depicting a marker chromosome, 47,XY,+mar. (A) This was... | Download Scientific Diagram
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
