File:Fneur-11-613035-t001.jpg

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	Date/Time	Thumbnail	Dimensions	User	Comment
current	22:49, 12 October 2023		1,143 × 894 (460 KB)	commons>Ozzie10aaaa	Uploaded a work by Angela Peron, Ilaria Catusi, Maria Paola Recalcati, Luciano Calzari, Lidia Larizza, Aglaia Vignoli, Maria Paola Canevini from https://www.frontiersin.org/articles/10.3389/fneur.2020.613035/full with UploadWizard

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Image title	Ring chromosome 20 [r(20)] syndrome is a rare condition characterized by a non-supernumerary ring chromosome 20 replacing a normal chromosome 20.
Author	Angela Peron
Short title	Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
Orientation	Normal
Horizontal resolution	72 dpi
Vertical resolution	72 dpi
Software used	Adobe Photoshop CS6 (Windows)
File change date and time	16:07, 2 December 2020
Color space	Uncalibrated
Date and time of digitizing	22:56, 1 December 2020
Date metadata was last modified	21:37, 2 December 2020
Unique ID of original document	uuid:b4452138-f587-45df-99cd-9495965787f8
Keywords	ring chromosome 20 syndrome r(20) ring chromosomes mosaicism cytogenetics karyotype seizures rare disease epilepsy