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Genomics|December 1, 1994
Characterization of 10 new polymorphic dinucleotide repeats and generation of a high-density microsatellite-based physical map of the BRCA1 region of chromosome 17q21F J Couch, S Kiousis, L H Castilla, et al.
Nature Genetics|December 30, 1999
MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instabilityS M Lipkin, V Wang, R Jacoby, et al.
American Journal of Human Genetics|May 1, 1989
Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8M C Iannuzzi, M Dean, M L Drumm, et al.
Genome Research|October 1, 1995
Approach to genotyping errors caused by nontemplated nucleotide addition by Taq DNA polymeraseJ R Smith, J D Carpten, M J Brownstein, et al.
Molecular and Cellular Biology|January 1, 1993
A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activityL B Andersen, R Ballester, D A Marchuk, et al.
Blood|February 1, 1990
The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factorsD L Gumucio, W K Lockwood, J L Weber, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1992
Sequencing and analysis of genomic fragments from the NF1 locusA Martin-Gallardo, D A Marchuk, J Gocayne, et al.
Human Mutation|January 1, 1992
Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) geneT V Strong, L S Smit, S Nasr, et al.
The American Journal of Pathology|November 1, 1994
Characterization of naturally occurring cutaneous neurofibromatosis in Holstein cattle. A disorder resembling neurofibromatosis type 1 in humansE A Sartin, S E Doran, M G Riddell, et al.
Genomics|July 15, 1996
A 500-kb physical map and contig from the Harvey ras-1 gene to the 11p telomereM W Russell, D J Munroe, E Bric, et al.
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