PDF) The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities
Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child | Journal of Medical Genetics
Chromosome Abnormality - an overview | ScienceDirect Topics
A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7
Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis | Molecular Cytogenetics | Full Text
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping
Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text
Abnormalities | Basicmedical Key
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
Ring chromosome - Wikipedia
Small supernumerary marker chromosome - Wikipedia
Numerical Abnormalities of Chromosomes Caused by the Electric Cha
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text
منظمة الصحة العالمية | المكتب الإقليمي لشرق المتوسط | Chromosomal aberrations in children with suspected genetic disorders | المجلد 3, العدد 1 | المجلة الصحية لشرق المتوسط - المجلد 3, 1997
Chromosome Marker - an overview | ScienceDirect Topics
![Karyotype of the patient with Marker chromosome : 47,XY,+mar[3]/46,XY[12] | Download Scientific Diagram](https://www.researchgate.net/publication/264008326/figure/fig5/AS:646465663795201@1531140833647/Karyotype-of-the-patient-with-Marker-chromosome-47-XY-mar3-46-XY12.png "Karyotype of the patient with Marker chromosome : 47,XY,+mar[3]/46,XY[12] | Download Scientific Diagram")
Karyotype of the patient with Marker chromosome : 47,XY,+mar[3]/46,XY[12] | Download Scientific Diagram
