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File:Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s007.ogv

Uncovering-Genomic-Causes-of-Co-Morbidity-in-Epilepsy-Gene-Driven-Phenotypic-Characterization-of-pone.0023182.s007.ogv ‎(Ogg Theora video file, length 1.9 s, 432 × 252 pixels, 501 kbps, file size: 115 KB)

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English: Animations of face morphs. Animations of face morphs offer the best visualisation of face shape differences when comparing each case and its age/sex-matched mean face. The unusual narrowness of Case 3's face is dysmorphic. S2 - Case 2.
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Source Video S2 from Kasperavičiūtė D, Catarino C, Chinthapalli K, Clayton L, Thom M, Martinian L, Cohen H, Adalat S, Bockenhauer D, Pope S, Lench N, Koltzenburg M, Duncan J, Hammond P, Hennekam R, Land J, Sisodiya S (2011). "Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions". PLOS ONE. DOI:10.1371/journal.pone.0023182. PMID 21858020. PMC: 3157359.
Author Kasperavičiūtė D, Catarino C, Chinthapalli K, Clayton L, Thom M, Martinian L, Cohen H, Adalat S, Bockenhauer D, Pope S, Lench N, Koltzenburg M, Duncan J, Hammond P, Hennekam R, Land J, Sisodiya S
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Date/TimeThumbnailDimensionsUserComment
current03:22, 14 November 20121.9 s, 432 × 252 (115 KB)Open Access Media Importer Bot (talk | contribs)Automatically uploaded media file from Open Access source. Please report problems or suggestions here.

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Format Bitrate Download Status Encode time
VP9 240P 170 kbps Completed 19:19, 24 October 2018 2.0 s
Streaming 240p (VP9) 172 kbps Completed 08:50, 21 December 2023 1.0 s
WebM 360P 296 kbps Completed 20:02, 2 December 2023 1.0 s
Streaming 144p (MJPEG) 510 kbps Completed 16:33, 11 November 2023 1.0 s

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