Mosaic trisomy (8)(p22 ? pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference26 articles.
1. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.
2. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization
3. Forty four probands with an additional ?marker? chromosome
4. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes
5. Domain Organization at the Centromere and Neocentromere
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1. Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis;Molecular Cytogenetics;2011
2. Inverted duplications on acentric markers: mechanism of formation;Human Molecular Genetics;2009-03-31
3. Neocentromeres: New Insights into Centromere Structure, Disease Development, and Karyotype Evolution;The American Journal of Human Genetics;2008-02
4. Characterization of rearrangements involving 4q, 13q and 16q in hepatocellular carcinoma cell lines using region-specific multiplex-FISH probes;Cancer Letters;2007-05
5. A neocentromere derived from a supernumerary marker deleted from the long arm of chromosome 6;Cytogenetic and Genome Research;2007
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