![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
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
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
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
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
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
![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
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
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
FISH with centromere-specific DNA probe D15Z4 (red signals) on a... | Download Scientific Diagram
Epigenetic Interface of Autism Spectrum Disorders (ASDs): Implications of Chromosome 15q11–q13 Segment | ACS Chemical Neuroscience
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports
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
Karyotype depicting a marker chromosome, 47,XY,+mar. (A) This was... | Download Scientific Diagram
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
Chromosome Marker - an overview | ScienceDirect Topics
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
A patient with a supernumerary marker chromosome (15), Angelman syndrome, and uniparental disomy resulting from paternal meiosis II non-disjunction | Journal of Medical Genetics
