A new neocentromere locus on chromosome 13 resulting in mosaic tetrasomy for distal 13q and an asymmetric phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference11 articles.
1. Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres
2. Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA
3. Chromosome 13q neocentromeres: Molecular cytogenetic characterization of three additional cases and clinical spectrum
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Prenatal identification of an inverted duplicated 13q marker chromosome with a neocentromere;Molecular Cytogenetics;2023-11-30
2. Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl;Frontiers in Genetics;2022-07-19
3. Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency;Birth Defects Research Part A: Clinical and Molecular Teratology;2015-04
4. Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations;American Journal of Medical Genetics Part A;2012-03-14
5. Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty;American Journal of Medical Genetics Part A;2009-03-30
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