Cargando…

Correction: Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

Detalles Bibliográficos
Autores principales:	Kitsiou-Tzeli, Sofia, Manolakos, Emmanouil, Lagou, Magdalini, Anagnostopoulou, Katerina, Kontodiou, Maria, Kosyakova, Nadezda, Ewers, Elisabeth, Weise, Anja, Garas, Antonios, Orru, Sandro, Liehr, Thomas, Metaxotou, Aikaterini
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2009
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651902/ https://www.ncbi.nlm.nih.gov/pubmed/19232114 http://dx.doi.org/10.1186/1755-8166-2-8

Ejemplares similares

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)

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

A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics
por: Lagou, Magdalini, et al.
Publicado: (2014)

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

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report
por: Manolakos, Emmanouil, et al.
Publicado: (2008)

Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature
por: Sifakis, Stavros, et al.
Publicado: (2012)

Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them
por: Liehr, Thomas, et al.
Publicado: (2008)

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)

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

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

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

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

Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature
por: MANOLAKOS, EMMANOUIL, et al.
Publicado: (2014)

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)
por: Manolakos, Emmanouil, et al.
Publicado: (2009)

The use of array-CGH in a cohort of Greek children with developmental delay
por: Manolakos, Emmanouil, et al.
Publicado: (2010)

Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male
por: Papoulidis, Ioannis, et al.
Publicado: (2015)

Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?
por: Polityko, Anna, et al.
Publicado: (2010)

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)

Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
por: Sismani, Carolina, et al.
Publicado: (2008)

Clinical Impact of Proximal Autosomal Imbalances
por: Hamid, AB, et al.
Publicado: (2012)

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
por: Manolakos, Emmanouil, et al.
Publicado: (2011)

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
por: Manolakos, Emmanouil, et al.
Publicado: (2011)

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

The Human Genome Puzzle – the Role of Copy Number Variation in Somatic Mosaicism
por: Mkrtchyan, Hasmik, et al.
Publicado: (2010)

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

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)

Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report
por: Fernández-Toral, Joaquín, et al.
Publicado: (2010)

De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features
por: Varvagiannis, Konstantinos, et al.
Publicado: (2014)

First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae)
por: Xiaobo, Fan, et al.
Publicado: (2013)

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

Position effect, cryptic complexity, and direct gene disruption as disease mechanisms in de novo apparently balanced translocation cases
por: Aristidou, Constantia, et al.
Publicado: (2018)

De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
por: Matsubara, Keiko, et al.
Publicado: (2020)

Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review
por: Liehr, Thomas, et al.
Publicado: (2019)

New cytogenetically visible copy number variant in region 8q21.2
por: Manvelyan, Marina, et al.
Publicado: (2011)

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

Supernumerary Staff
Publicado: (1965)

Supernumerary Teeth
Publicado: (1859)

An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4
por: Selenti, Nikoletta, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_g5q6upnb5alq0dhggapc10bsgg