IJMS | Free Full-Text | Chromosomal Microarray Study in Prader-Willi Syndrome
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 systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
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
Neurodevelopmental Disorders Associated with Chromosome 15
Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians | SpringerLink
![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
FISH with centromere-specific DNA probe D15Z4 (red signals) on a... | Download Scientific Diagram
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
Karyotype depicting a marker chromosome, 47,XY,+mar. (A) This was... | Download Scientific Diagram
Small supernumerary marker chromosome - Wikipedia
A patient with a supernumerary marker chromosome (15), Angelman syndrome, and uniparental disomy resulting from paternal meiosis II non-disjunction | Journal of Medical Genetics
Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text
Chromosome 15 - Wikipedia
Genetics of AS – Angelman Syndrome Foundation
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
![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
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
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports
Chromosome 15 - Wikiwand
Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features
![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
Chromosome Marker - an overview | ScienceDirect Topics
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
