NF2 & Gorlins [electronic resource] / D. Gareth R. Evans.

By: Evans, D. Gareth R [spk]Material type: FilmFilmSeries: Henry Stewart talksBiomedical & life sciences collection. Molecular genetics of human disease: Publisher: London : Henry Stewart Talks, 2014Description: 1 online resource (1 streaming video file (52 min.) : color, sound)Other title: Neurofibromatosis 2 and GorlinsSubject(s): Cancer -- Genetic aspects | Genetic disorders | Head -- Abnormalities | Medical genetics | Neck -- Abnormalities | Nervous system -- Diseases -- Genetic aspects | Neurofibromatosis | Basal Cell Nevus Syndrome | Cerebellar Neoplasms -- genetics | Genes, Neurofibromatosis 2 | Genetics, Medical | Meningeal Neoplasms -- genetics | Neoplastic Syndromes, Hereditary -- genetics | Nervous System Neoplasms -- genetics | Neurofibromatosis 2 -- genetics | Neurofibromatosis 2 -- pathologyOnline resources: Click here to access online | Series
Contents:
Contents: NF2 -- An autosomal dominant inherited tumours predisposition syndrome -- Bilateral vestibular schwannomas -- Schwannomas of other cranial and spinal nerve routes -- Meningiomas -- Ependymomas affected mainly the upper spine -- Cataracts -- Mutations in the NF2 gene Gorlin syndrome -- An autosomal dominant inherited tumours predisposition syndrome -- Multiple BCCs -- Jaw keratocysts -- Medulloblastoma -- Mutations in the PTCH gene.
Tags from this library: No tags from this library for this title. Log in to add tags.
    Average rating: 0.0 (0 votes)
No physical items for this record

Animated audio-visual presentation with synchronized narration.

Title from title frames.

Contents: NF2 -- An autosomal dominant inherited tumours predisposition syndrome -- Bilateral vestibular schwannomas -- Schwannomas of other cranial and spinal nerve routes -- Meningiomas -- Ependymomas affected mainly the upper spine -- Cataracts -- Mutations in the NF2 gene Gorlin syndrome -- An autosomal dominant inherited tumours predisposition syndrome -- Multiple BCCs -- Jaw keratocysts -- Medulloblastoma -- Mutations in the PTCH gene.

Access restricted to subscribers.

Mode of access: World Wide Web.

Technical University of Mombasa
Tom Mboya Street, Tudor 90420-80100 , Mombasa Kenya
Tel: (254)41-2492222/3 Fax: 2490571