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Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum.
Çakmaklı S, Çankaya T, Gürsoy S, Koç A, Kırbıyık Ö, Kılıçarslan ÖA, Özer E, Erçal D, Bozkaya ÖG. Çakmaklı S, et al. Cytogenet Genome Res. 2017;153(4):175-180. doi: 10.1159/000486775. Epub 2018 Mar 9. Cytogenet Genome Res. 2017. PMID: 29518772 Review.
Monosomy and ring chromosome 13 in a thyroid nodular goiter-do we underestimate its relevance in benign thyroid lesions?
Sendt W, Rippe V, Flor I, Drieschner N, Bullerdiek J. Sendt W, et al. Cancer Genet. 2012 Mar;205(3):128-30. doi: 10.1016/j.cancergen.2012.01.010. Cancer Genet. 2012. PMID: 22469512
They were characterized by monosomy 13 as the sole abnormality in one clone, and loss of one chromosome 13 and a ring chromosome that was found to consist of chromosome 13 material by fluorescence in situ hybridization in the other clone. We have concluded that during the cour …
They were characterized by monosomy 13 as the sole abnormality in one clone, and loss of one chromosome 13 and a ring chromosome that was fo …
The ring chromosome 13 syndrome.
Martin NJ, Harvey PJ, Pearn JH. Martin NJ, et al. Hum Genet. 1982;61(1):18-23. doi: 10.1007/BF00291324. Hum Genet. 1982. PMID: 7129419