neurofibromatosis

n.

神经纤维瘤病；

1. ObjectiveTo study the diagnosis and therapy of hereditary neurofibromatosis.
   目的探讨多发性神经纤维瘤病的家族遗传性及诊断治疗的进展。

Von Recklinghausen neurofibromatosis.
The neurofibromatosis type 1 gene encodes a protein related to GAP.
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
Malignant peripheral nerve sheath tumours in neurofibromatosis 1
The GAP-related domain of the neurofibromatosis type 1 gene product interacts with p21
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17
A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations.
Common Pathogenetic Mechanism for Three Tumor Types in Bilateral Acoustic Neurofibromatosis
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor