Cargando…

Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them

BACKGROUND: Small supernumerary marker chromosomes (sSMC) and B-chromosomes represent a heterogeneous collection of chromosomes added to the typical karyotype, and which are both small in size. They may consist of heterochromatic and/or euchromatic material. Also a predominance of maternal transmiss...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liehr, Thomas, Mrasek, Kristin, Kosyakova, Nadezda, Ogilvie, Caroline Mackie, Vermeesch, Joris, Trifonov, Vladimir, Rubtsov, Nikolai
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2008
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2427039/ https://www.ncbi.nlm.nih.gov/pubmed/18533011 http://dx.doi.org/10.1186/1755-8166-1-12

Ejemplares similares

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?
por: Trifonov, Vladimir, et al.
Publicado: (2008)

Characterization of prenatally detected small Supernumerary Marker Chromosomes (sSMC) by molecular cytogenetic technique: FISH
por: Patel, Bhumi, et al.
Publicado: (2014)

A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC)
por: Domaradzka, Justyna, et al.
Publicado: (2021)

Whole Exome Sequencing Facilitated the Identification of a Mosaic Small Supernumerary Marker Chromosome (sSMC)
por: Xing, Huan-xia, et al.
Publicado: (2021)

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes
por: Liehr, Thomas, et al.
Publicado: (2010)

Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report
por: Abdullah,, et al.
Publicado: (2021)

Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient
por: Olszewska, Marta, et al.
Publicado: (2015)

The hierarchically organized splitting of chromosomal bands for all human chromosomes
por: Kosyakova, Nadezda, et al.
Publicado: (2009)

A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report
por: Sheth, Frenny, et al.
Publicado: (2009)

Complex small supernumerary marker chromosomes – an update
por: Liehr, Thomas, et al.
Publicado: (2013)

Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishes
por: Cioffi, Marcelo B, et al.
Publicado: (2011)

Exploring Supernumeraries - A New Marker for Screening of B-Chromosomes Presence in the Yellow Necked Mouse Apodemus flavicollis
por: Bugarski-Stanojević, Vanja, et al.
Publicado: (2016)

Evolution, Composition and Regulation of Supernumerary B Chromosomes
por: Houben, Andreas, et al.
Publicado: (2019)

Small supernumerary marker chromosomes – an update
por: Liehr, Thomas
Publicado: (2014)

A De Novo sSMC (22) Characterized by High-Resolution Chromosome Microarray Analysis in a Chinese Boy with Cat-Eye Syndrome
por: Li, Jinjie, et al.
Publicado: (2021)

Early Embryonic Chromosome Instability Results in Stable Mosaic Pattern in Human Tissues
por: Mkrtchyan, Hasmik, et al.
Publicado: (2010)

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
por: Kitsiou-Tzeli, Sofia, et al.
Publicado: (2009)

Small supernumerary marker chromosomes derived from chromosome 14 and/or 22
por: Liehr, Thomas, et al.
Publicado: (2021)

Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
por: Karamysheva, Tatyana V., et al.
Publicado: (2020)

Correction: Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
por: Kitsiou-Tzeli, Sofia, et al.
Publicado: (2009)

Small supernumerary marker chromosomes and their correlation with specific syndromes
por: Jafari-Ghahfarokhi, Hamideh, et al.
Publicado: (2015)

New Insights into Phasmatodea Chromosomes
por: Liehr, Thomas, et al.
Publicado: (2017)

Genomic and transcriptomic profiling of resistant CEM/ADR-5000 and sensitive CCRF-CEM leukaemia cells for unravelling the full complexity of multi-factorial multidrug resistance
por: Kadioglu, Onat, et al.
Publicado: (2016)

Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines
por: Lopez Corrales, Nestor Luis, et al.
Publicado: (2012)

Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic features
por: Stavber, Lana, et al.
Publicado: (2017)

Generation of multicolor banding probes for chromosomes of different species
por: Kosyakova, Nadezda, et al.
Publicado: (2013)

Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics
por: Klein, Elisabeth, et al.
Publicado: (2012)

Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing
por: Zlotina, Anna, et al.
Publicado: (2016)

A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndrome
por: Haltrich, Irén, et al.
Publicado: (2014)

The bacterial chromosome: architecture and action of bacterial SMC and SMC-like complexes
por: Nolivos, Sophie, et al.
Publicado: (2014)

Be careful with small supernumerary marker chromosomes!
por: Rodríguez, Laura
Publicado: (2023)

Sequencing of Supernumerary Chromosomes of Red Fox and Raccoon Dog Confirms a Non-Random Gene Acquisition by B Chromosomes
por: Makunin, Alexey I., et al.
Publicado: (2018)

First Molecular Cytogenetic High Resolution Characterization of the NIH 3T3 Cell Line by Murine Multicolor Banding
por: Leibiger, Christine, et al.
Publicado: (2013)

New Insights Into Chromomere Organization Provided by Lampbrush Chromosome Microdissection and High-Throughput Sequencing
por: Zlotina, Anna, et al.
Publicado: (2020)

The Smc5–Smc6 Complex Is Required to Remove Chromosome Junctions in Meiosis
por: Farmer, Sarah, et al.
Publicado: (2011)

Chromosomal phenotypes and submicroscopic abnormalities
por: Devriendt, Koen, et al.
Publicado: (2004)

The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
por: Weber, André, et al.
Publicado: (2022)

Small Supernumerary Marker Chromosome May Provide Information on Dosage-insensitive Pericentric Regions in Human
por: Al-Rikabi, Ahmed B. Hamid, et al.
Publicado: (2018)

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing
por: Lebedev, Igor N., et al.
Publicado: (2021)

Discovery of Supernumerary B Chromosomes in Drosophila melanogaster
por: Bauerly, Elisabeth, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_7brhkkk0if2nf5vnmgobonepm2