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Genes, Chromosomes & Cancer|September 1, 1996
Frequency and distribution of NF2 mutations in schwannomasL B Jacoby, M MacCollin, R Barone, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1982
Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequencesJ F Gusella, C Jones, F T Kao, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1988
Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21N Sacchi, J F Gusella, L Perroni, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1992
Immunohistochemical localization of the D1 dopamine receptor in rat brain reveals its axonal transport, pre- and postsynaptic localization, and prevalence in the basal ganglia, limbic system, and thalamic reticular nucleusQ Huang, D Zhou, K Chase, et al.
Neuromuscular Disorders : NMD|January 1, 1996
Hypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effectC L Grosson, J Esteban, D McKenna-Yasek, et al.
Human Molecular Genetics|June 1, 1993
Mouse neurofibromatosis type 1 cDNA sequence reveals high degree of conservation of both coding and non-coding mRNA segmentsA Bernards, A J Snijders, G E Hannigan, et al.
Human Mutation|January 1, 1992
A 15-bp deletion in exon 5 of the ornithine aminotransferase (OAT) locus associated with gyrate atrophyJ K Park, J J O'Donnell, V E Shih, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
The alpha-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse chromosome 11C Ambrose, S Cheng, B Fontaine, et al.
Developmental Neuroscience|January 1, 1987
Models for inherited susceptibility to cancer in the nervous system: a molecular-genetic approach to neurofibromatosisB R Seizinger, R L Martuza, G Rouleau, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1988
Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21D Patterson, K Gardiner, F T Kao, et al.
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