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Neurofibromatosis type 1 (NF1) is one of the commonest autosomal disorders in man with an estimated birth incidence of 1/2500 (Crowe et al., 1956; Huson et al., 1989a).
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Key Phrases - Statistically Improbable Phrases (SIPs):
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ira mutant yeast, neurofibromin expression, ras affinity, express neurofibromin, human neurofibromin, mice exhibit activation, neurofibromin distribution, nfl gene, nfl mutations, neurofibroma formation, suppressor hypothesis, nfl locus, neurofibromin results, neurofibromin isoforms, peripheral nerve sheath tumours, show somatic deletions, malignant myeloid disorders, neurofibromatosis type, perineurial cells, neurofibromatosis gene, complements ira mutants, dermal neurofibroma, embedded genes, ras interaction, optic pathway gliomas
Key Phrases - Capitalized Phrases (CAPs):
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Nature Genet, New Engl, Genetic Analysis Consortium, National Neurofibromatosis Foundation, Scientific Publishers Ltd, Cell Biol, New York, Cancer Res, Genes Dev, Introduction Neurofibromatosis, Nucleic Acids Res, Brain Res, Cancer Genet, Acta Neuropathol, Genes Chromosomes Cancer, Requirement of Drosophila, Consensus Conference, South Wales, University of Utah, Cell Genet, Child Neural, Genes Chront, Johns Hopkins University Press, Oxford University Press
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