Article
Combined molecular genetic studies of chromosome 22q and the neurofibromatosis type 2 gene in central nervous system tumors.
Neurosurgery - 1 Oct 1995
Ng H K, Lau K M, Tse J Y, Lo K W, Wong J H, Poon W S, Huang D P
Abstract excerpt
Monosomy of chromosome 22 or deletions of 22q have been described in meningiomas and astrocytic tumors, the incidence of which is increased in Type 2 neurofibromatosis. Recently, the gene for neurofibromatosis Type 2 (NF2) has been identified at Chromosome 22q12, and a tumor suppression role has been suggested. Because there have been only a few studies of the NF2 gene on central nervous system tumors other than...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
