Identification of a ring chromosome as a ring 8 using fluorescent in situ hybridization (FISH) in a child with multiple congenital anomalies
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference5 articles.
1. Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies
2. A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)
3. Pericentric inversion of chromosome 7 (inv(7) (p22q11.2)) and ring chromosome 8 (r(8) (p23q24.3)) in a girl with minor anomalies.
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1. First case of two supernumerary markers derived from chromosome 5 and chromosome 8;Molecular Cytogenetics;2022-06-27
2. 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
3. Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8,18, and 21 in three patients;Journal of Applied Genetics;2007-06
4. Characterization of a small supernumerary marker chromosome as r(8) at prenatal diagnosis by MFISH;Prenatal Diagnosis;2005-01
5. Supernumerary ring chromosome 8: Clinical and molecular cytogenetic characterization in a case report;American Journal of Medical Genetics;2004
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