Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15. | Semantic Scholar
Paternal Transmission of Small Supernumerary Marker Chromosome 15 Identified in Prenatal Diagnosis Due to Advanced Maternal Age
Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text
Molecular cytogenetic characterization of an isodicentric Yq and a neocentric isochromosome Yp in an azoospermic male
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
How common is isodicentric chromosome 15 syndrome?
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome - ScienceDirect
![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
SciELO - Brasil - Mosaic 15q duplication syndrome (tetrasomy 15q11.1-q13.2) in a child with behavior disorders: case report Mosaic 15q duplication syndrome (tetrasomy 15q11.1-q13.2) in a child with behavior disorders: case report
Chromosome 15 - Wikiwand
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
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
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
Chromosome 15: Human Genome Landmarks Poster
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping
Frontiers | Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
Karyotype showing marker chromosome. | Download Scientific Diagram
FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22) | European Journal of Human Genetics
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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
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
A patient with a supernumerary marker chromosome (15), Angelman syndrome, and uniparental disomy resulting from paternal meiosis II non-disjunction | Journal of Medical Genetics
