Small supernumerary marker chromosome - Wikipedia
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping
Marker Chromosomes | SpringerLink
Figure 1.3 from Small supernumerary marker chromosomes (sSMC) : why do they break, where they break and how to distinguish harmful from harmless sSMC? | Semantic Scholar
Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report
Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text
Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
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
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
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
menetrend Várj egy percet Levelek gyűjtése marker cromosom És a csapat Confuse Plüss Doll
menetrend Várj egy percet Levelek gyűjtése marker cromosom És a csapat Confuse Plüss Doll
![PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0653e5cd80daeba739f8717a277fed33064ad223/3-Figure1-1.png "PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic Scholar")
PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic Scholar
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
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Case 613 -- Cytogenetics - Pathology Case
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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
Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report - Abdullah - Translational Andrology and Urology
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Marker Chromosome - an overview | ScienceDirect Topics
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
Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl | Journal of Medical Genetics
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text
