Research Story Tip: Genetic Marker for Prostate Cancer Found to Be Common Among Black Males
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping
A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics
Molecular Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Chromosome Y in an Infertile Male with Apparently Normal Phenotype: A Case Report and Literature Review
Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome | Molecular Cytogenetics | Full Text
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities - ScienceDirect
A novel translocation der(4)t(1;4)(q21;q35) and a marker chromosome in a case of myelodysplastic syndrome - Cancer Genetics and Cytogenetics
G-banded karyotype showing the marker chromosome. | Download Scientific Diagram
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 mosaicism for a small supernumerary marker chromosome derived from chromosome 11 - ScienceDirect
Case Reports r8p23q24AshokID100089
CHARACTERISATION OF MARKER CHROMOSOMES | PharmaTutor
Diagnostics | Free Full-Text | Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15. | Semantic Scholar
Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
SciELO - Brasil - Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with
A karyotype of 47,XX,þmar. The arrow indicates a marker chromosome (mar). | Download Scientific Diagram
The G-banded karyotype. mar = marker chromosome. | Download Scientific Diagram
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A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
