neurofibromatosis
英 [njʊə'rəʊfaɪbrəʊmətəʊsɪs] 美 [njʊr'roʊfaɪbroʊmətoʊsɪs]

n.

神经纤维瘤病；

英英释义

neurofibromatosis[ ,njuərəufi,brəumə'təusis ]

• n.autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities

  同义词：von Recklinghausen's disease

双语例句

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。

权威例句

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