Neurofibromatosis type 1 : from genotype to phenotype
Author(s)
Bibliographic Information
Neurofibromatosis type 1 : from genotype to phenotype
Bios Scientific, 1998
Available at 3 libraries
  Aomori
  Iwate
  Miyagi
  Akita
  Yamagata
  Fukushima
  Ibaraki
  Tochigi
  Gunma
  Saitama
  Chiba
  Tokyo
  Kanagawa
  Niigata
  Toyama
  Ishikawa
  Fukui
  Yamanashi
  Nagano
  Gifu
  Shizuoka
  Aichi
  Mie
  Shiga
  Kyoto
  Osaka
  Hyogo
  Nara
  Wakayama
  Tottori
  Shimane
  Okayama
  Hiroshima
  Yamaguchi
  Tokushima
  Kagawa
  Ehime
  Kochi
  Fukuoka
  Saga
  Nagasaki
  Kumamoto
  Oita
  Miyazaki
  Kagoshima
  Okinawa
  Korea
  China
  Thailand
  United Kingdom
  Germany
  Switzerland
  France
  Belgium
  Netherlands
  Sweden
  Norway
  United States of America
Note
Includes bibliographies and index
Description and Table of Contents
Description
Neurofibromatosis type 1 (NF1) is a common disease affecting 1 in 4000 individuals world-wide. Symptoms include facial and body disfigurement, mental retardation and abnormalities of the cardiovascular, renal and endocrine systems. The book begins with
Table of Contents
- Neurofibromatosis type 1: historical perspective and introductory
- overview
- Clinical aspects of neurofibromatosis 1
- Gene structure and expression
- The NF1 Genetic Analysis Consortium
- The mutational spectrum in neurofibromatosis 1 and its underlying me
by "Nielsen BookData"