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A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7
PDF) The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities
Prenatal chromosomal microarray analysis in 2466 fetuses with ultrasonographic soft markers: a prospective cohort study - American Journal of Obstetrics & Gynecology
Small supernumerary marker chromosome - Wikipedia
Chromosome Marker - an overview | ScienceDirect Topics
Ring chromosome - Wikipedia
Karyotype showing marker chromosome. | Download Scientific Diagram
Acquired chromosome abnormalities: the cytogenetics of cancer (Genetics)
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians | SpringerLink
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | 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
Genes | Free Full-Text | Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis | Molecular Cytogenetics | Full Text
![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
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
Chromosome Abnormality - an overview | ScienceDirect Topics
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | Genetics in Medicine
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
Numerical Abnormalities of Chromosomes Caused by the Electric Cha
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
Abnormalities | Basicmedical Key
Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child | Journal of Medical Genetics
Neocentromere - Wikipedia
