A neocentromere derived from a supernumerary marker deleted from the long arm of chromosome 6
Author:
Publisher
S. Karger AG
Subject
Genetics(clinical),Genetics,Molecular Biology
Reference12 articles.
1. Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres
2. Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3
3. Interstitial deletion 11(p11.12p11.2) and analphoid marker formation results in inherited Potocki-Shaffer syndrome
4. Mosaic trisomy (8)(p22 ? pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences
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1. A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15;American Journal of Medical Genetics Part A;2016-10-14
2. 6q16.3q23.3 duplication associated with Prader-Willi-like syndrome;Molecular Cytogenetics;2015-06-25
3. De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features;Gene;2013-07
4. Reestructuraciones compatibles con un fenotipo normal detectadas en diagnóstico prenatal;Diagnóstico Prenatal;2013-07
5. Centromeres: Old tales and new tools;FEBS Letters;2008-04-22
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