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Treacher Collins Syndrome

dc.contributor.authorHassouna, Alla
dc.date.accessioned2019-08-07T09:24:31Z
dc.date.available2019-08-07T09:24:31Z
dc.date.issued2019-05-04
dc.identifier.urihttp://repository.limu.edu.ly/handle/123456789/1120
dc.descriptionTreacher Collins syndrome is a condition that affects the development of bones and other tissues of the face. The signs and symptoms of this disorder vary greatly, ranging from almost unnoticeable to severe. it caused by abnormal development of the facial 1 st and 2 nd pharyngeal arches . its an autosomal dominant genetic disorder which is caused by mutation in chromosome 5 {5q32-33 } in gene TCOF1 called treacle.en_US
dc.language.isoenen_US
dc.publisherfaculty of Basic Medical Science - Libyan International Medical Universityen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.titleTreacher Collins Syndromeen_US
dc.typeOtheren_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States