A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
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
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Genetics of AS – Angelman Syndrome Foundation
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
Chromosome 15 - Wikiwand
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
A patient with a supernumerary marker chromosome (15), Angelman syndrome, and uniparental disomy resulting from paternal meiosis II non-disjunction | Journal of Medical Genetics
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
IJMS | Free Full-Text | Chromosomal Microarray Study in Prader-Willi Syndrome
FISH with centromere-specific DNA probe D15Z4 (red signals) on a... | 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
![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
Karyotype depicting a marker chromosome, 47,XY,+mar. (A) This was... | Download Scientific Diagram
Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature | Journal of Medical Case Reports | Full Text
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
Small supernumerary marker chromosome - Wikipedia
Chromosome Marker - an overview | ScienceDirect Topics
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
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 supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype | Journal of Medical Genetics
Supernumerary Marker of Chromosome 15 Associated with Paternal Uniparental Disomy in a Case with Angelman Syndrome
