Interstitial Deletion of Proximal 8q Including Part of the Centromere from Unbalanced Segregation of a Paternal Deletion/Marker Karyotype with Neocentromere Formation at 8p22
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics,Molecular Biology
Reference22 articles.
1. Human centromere repositioning "in progress"
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3. Proximal chromosome 8q deletion in a boy with femoral bifurcation and other multiple congenital anomalies
4. Mechanisms and Consequences of Small Supernumerary Marker Chromosomes: From Barbara McClintock to Modern Genetic-Counseling Issues
5. Complementary duplication and deletion of 17 (pcen→p11.2): A family with a supernumerary chromosome comprised of an interstitially deleted segment
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1. The dark side of centromeres: types, causes and consequences of structural abnormalities implicating centromeric DNA;Nature Communications;2018-10-18
2. Neocentromeres to the Rescue of Acentric Chromosome Fragments;Molecular Syndromology;2017
3. The incidence of chromosome abnormalities in neonates with structural heart disease;Heart;2016-02-03
4. Neocentromeres and epigenetically inherited features of centromeres;Chromosome Research;2012-06-22
5. Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing;Cytogenetic and Genome Research;2012
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