Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference30 articles.
1. Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation
2. A case of apparent trisomy 21 without the Down's syndrome phenotype.
3. An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite
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1. A 15 Mb large paracentric chromosome 21 inversion identified in Czech population through a pair of flanking duplications;Molecular Cytogenetics;2014-08-19
2. Neocentric Small Supernumerary Marker Chromosomes by Chromosome;Small Supernumerary Marker Chromosomes (sSMC);2011-06-19
3. Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22;American Journal of Medical Genetics Part A;2011-06-10
4. A case of Down syndrome with mirror-image duplication of chromosome 21;American Journal of Medical Genetics Part A;2010
5. Neocentromeres: New Insights into Centromere Structure, Disease Development, and Karyotype Evolution;The American Journal of Human Genetics;2008-02
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