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Genetic Epidemiology|January 1, 1987
Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysisP L Kramer, L Ozelius, J F Gusella, et al.
American Journal of Medical Genetics|November 20, 1995
Prenatal diagnosis of familial dysautonomia by analysis of linked CA-repeat polymorphisms on chromosome 9q31-q33C M Eng, S A Slaugenhaupt, A Blumenfeld, et al.
American Journal of Human Genetics|July 1, 1993
The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HDL A Farrer, L A Cupples, P Wiater, et al.
Neurogenetics|February 7, 2001
Allelic expression of the NF2 gene in neurofibromatosis 2 and schwannomatosisL B Jacoby, M MacCollin, D M Parry, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Different gene loci for hyperkalemic and hypokalemic periodic paralysisB Fontaine, J Trofatter, G A Rouleau, et al.
Genes & Development|May 30, 1998
Mice heterozygous for a mutation at the Nf2 tumor suppressor locus develop a range of highly metastatic tumorsA I McClatchey, I Saotome, K Mercer, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1980
Isolation and localization of DNA segments from specific human chromosomesJ F Gusella, C Keys, A VarsanyiBreiner, et al.
International Journal of Cancer|August 22, 1995
Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomasI Slavc, M M MacCollin, M Dunn, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 12, 1995
Molecular characterization of a second melatonin receptor expressed in human retina and brain: the Mel1b melatonin receptorS M Reppert, C Godson, C D Mahle, et al.
The Journal of Experimental Medicine|June 1, 1980
Erythroleukemia induction by replication-competent type C viruses cloned from the anemia- and polycythemia-inducing isolates of Friend leukemia virusM E MacDonald, T W Mak, A Bernstein
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