Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
Neurodevelopmental Disorders Associated with Chromosome 15
Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature | Journal of Medical Case Reports | Full Text
Supernumerary Marker of Chromosome 15 Associated with Paternal Uniparental Disomy in a Case with Angelman Syndrome
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
Chromosome 15 - Wikipedia
Karyotype depicting a marker chromosome, 47,XY,+mar. (A) This was... | Download Scientific Diagram
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
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
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
Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
Genetics of AS – Angelman Syndrome Foundation
Chromosome Marker - an overview | ScienceDirect Topics
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
Isodicentric 15 - Wikipedia
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians | SpringerLink