Publication date
January 1998
DOI Publisher
INIST-CNRS Journal
Atlas of Genetics and Cytogenetics in Oncology and HaematologyAbstract
Review on Neurofibromatosis type 2 (NF2), with data on clinics, and the genes involved
Review on Neurofibromatosis type 2 (NF2), with data on clinics, and the genes involved
Background: Neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2) are rare tumoral suppr...
The autosomal dominant syndrome neurofibromatosis type 2 (NF2) is characterized by the development o...
The 2011 annual meeting of the Children’s Tumor Foundation, the annual gathering of the neurofibroma...
Abstract Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development ...
Neurofibromatosis type 2 (NF2) is an autosomal dominant disease with the hallmark of bilateral vesti...
Review on Neurofibromatosis type 2 (NF2), with data on clinics, and the genes involved
Neurofibromatosis type 2 (NF2), a multiple neoplasia syndrome, is a manifestation of an impaired exp...
Neurofibromatosis 2 (NF2) is an autosomal dominant disease that is characterized by tumors on the ve...
Neurofibromatosis type 2 (NF2) is an autosomal domi-nant disorder that predisposes to nervous system...
SummaryPatients with multiple schwannomas without vestibular schwannomas have been postulated to com...
This is an open-access article distributed under the terms of the Creative Commons Attribution Licen...
Inactivating germline mutations in the tumor suppressor gene NF2 cause the hereditary syndrome neuro...
Introduction Neurofibromatosis type 2 (NF2) and schwannomatosis are entities that may, due to the si...
The 2011 annual meeting of the Children's Tumor Foundation, the annual gathering of the neurofibroma...
Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder with the clinical hallmark of bilat...
Background: Neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2) are rare tumoral suppr...
The autosomal dominant syndrome neurofibromatosis type 2 (NF2) is characterized by the development o...
The 2011 annual meeting of the Children’s Tumor Foundation, the annual gathering of the neurofibroma...
Abstract Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development ...
Neurofibromatosis type 2 (NF2) is an autosomal dominant disease with the hallmark of bilateral vesti...
Review on Neurofibromatosis type 2 (NF2), with data on clinics, and the genes involved
Neurofibromatosis type 2 (NF2), a multiple neoplasia syndrome, is a manifestation of an impaired exp...
Neurofibromatosis 2 (NF2) is an autosomal dominant disease that is characterized by tumors on the ve...
Neurofibromatosis type 2 (NF2) is an autosomal domi-nant disorder that predisposes to nervous system...
SummaryPatients with multiple schwannomas without vestibular schwannomas have been postulated to com...
This is an open-access article distributed under the terms of the Creative Commons Attribution Licen...
Inactivating germline mutations in the tumor suppressor gene NF2 cause the hereditary syndrome neuro...
Introduction Neurofibromatosis type 2 (NF2) and schwannomatosis are entities that may, due to the si...
The 2011 annual meeting of the Children's Tumor Foundation, the annual gathering of the neurofibroma...
Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder with the clinical hallmark of bilat...
Background: Neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2) are rare tumoral suppr...
The autosomal dominant syndrome neurofibromatosis type 2 (NF2) is characterized by the development o...
The 2011 annual meeting of the Children’s Tumor Foundation, the annual gathering of the neurofibroma...
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