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Genetic mapping of a second myotonic dystrophy locus.
Ranum LP, Rasmussen PF, Benzow KA, Koob MD, Day JW. Ranum LP, et al. Nat Genet. 1998 Jun;19(2):196-8. doi: 10.1038/570. Nat Genet. 1998. PMID: 9620781
Reply-.
Moseley ML, Schut LJ, Bird TD, Day JW, Ranum LP. Moseley ML, et al. Nat Genet. 2000 Mar;24(3):215. doi: 10.1038/73415. Nat Genet. 2000. PMID: 10700169 No abstract available.
Dominant non-coding repeat expansions in human disease.
Dick KA, Margolis JM, Day JW, Ranum LPW. Dick KA, et al. Genome Dyn. 2006;1:67-83. doi: 10.1159/000092501. Genome Dyn. 2006. PMID: 18724054 Review.
Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
Mosemiller AK, Dalton JC, Day JW, Ranum LP. Mosemiller AK, et al. Cytogenet Genome Res. 2003;100(1-4):175-83. doi: 10.1159/000072852. Cytogenet Genome Res. 2003. PMID: 14526178 Review.
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP. Liquori CL, et al. Science. 2001 Aug 3;293(5531):864-7. doi: 10.1126/science.1062125. Science. 2001. PMID: 11486088
Spinocerebellar ataxia type 8: clinical features in a large family.
Day JW, Schut LJ, Moseley ML, Durand AC, Ranum LP. Day JW, et al. Neurology. 2000 Sep 12;55(5):649-57. doi: 10.1212/wnl.55.5.649. Neurology. 2000. PMID: 10980728
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).
Koob MD, Moseley ML, Schut LJ, Benzow KA, Bird TD, Day JW, Ranum LP. Koob MD, et al. Nat Genet. 1999 Apr;21(4):379-84. doi: 10.1038/7710. Nat Genet. 1999. PMID: 10192387
Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).
Day JW, Roelofs R, Leroy B, Pech I, Benzow K, Ranum LP. Day JW, et al. Neuromuscul Disord. 1999 Jan;9(1):19-27. doi: 10.1016/s0960-8966(98)00094-7. Neuromuscul Disord. 1999. PMID: 10063831
We have recently mapped the disease locus (DM2) in this family to a 10 cM region of chromosome 3q [Ranum LPW, Rasmussen PF, Benzow KA, Koob MD, Day JW. ...
We have recently mapped the disease locus (DM2) in this family to a 10 cM region of chromosome 3q [Ranum LPW, Rasmussen PF, Benzow KA, Koob …
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA.
Koob MD, Benzow KA, Bird TD, Day JW, Moseley ML, Ranum LP. Koob MD, et al. Nat Genet. 1998 Jan;18(1):72-5. doi: 10.1038/ng0198-72. Nat Genet. 1998. PMID: 9425905
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