Supernumerary ring chromosome 8: Clinical and molecular cytogenetic characterization in a case report
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference26 articles.
1. Detailed characterization of 12 supernumerary ring chromosomes using micro‐FISH and search for uniparental disomy
2. Preferential involvement of the short arm in chromosome 8-derived supernumerary markers and ring as identified by chromosome arm painting
3. Identification of a ring chromosome as a ring 8 using fluorescent in situ hybridization (FISH) in a child with multiple congenital anomalies
4. Identification of marker chromosomes in thirteen patients using FISH probing
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1. Mosaic partial pericentromeric trisomy 8 and maternal uniparental disomy in a male patient with autism spectrum disorder;Clinical Case Reports;2016-10-21
2. A Novel 1.0 Mb Duplication of Chromosome 8p22-21.3 in a Patient With Autism Spectrum Disorder;Child Neurology Open;2015-06
3. Autism spectrum disorders: The quest for genetic syndromes;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2013-05-03
4. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis;Taiwanese Journal of Obstetrics and Gynecology;2012-09
5. Mosaicismo de trisomía parcial del cromosoma 8 asociado a tetralogía de Fallot;Anales de Pediatría;2011-01
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