Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
![PDF] Isodicentric Chromosome 15 Syndrome in a Korean Patient With Café-au-lait Spots | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/765486dbb8123ad8cf82b66bc59c4b152d3049fe/2-Figure2-1.png "PDF] Isodicentric Chromosome 15 Syndrome in a Korean Patient With Café-au-lait Spots | Semantic Scholar")
PDF] Isodicentric Chromosome 15 Syndrome in a Korean Patient With Café-au-lait Spots | Semantic Scholar
Genetics of AS – Angelman Syndrome Foundation
![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
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
Supernumerary Marker of Chromosome 15 Associated with Paternal Uniparental Disomy in a Case with Angelman Syndrome
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text
Frontiers | Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches
A patient with a supernumerary marker chromosome (15), Angelman syndrome, and uniparental disomy resulting from paternal meiosis II non-disjunction | Journal of Medical Genetics
Epigenetic Interface of Autism Spectrum Disorders (ASDs): Implications of Chromosome 15q11–q13 Segment | ACS Chemical Neuroscience
Chromosome 15 - Wikipedia
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
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
Karyotype depicting a marker chromosome, 47,XY,+mar. (A) This was... | Download Scientific Diagram
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
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 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
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
