Stauffer D - Search Results

1

Etiological heterogeneity in X-linked spastic paraplegia.

Keppen LD, Leppert MF, O'Connell P, Nakamura Y, Stauffer D, Lathrop M, Lalouel JM, White R. Keppen LD, et al. Among authors: stauffer d. Am J Hum Genet. 1987 Nov;41(5):933-43. Am J Hum Genet. 1987. PMID: 3479019 Free PMC article.

2

Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22.

Hoehe MR, Plaetke R, Otterud B, Stauffer D, Holik J, Byerley WF, Baetge EE, Gershon ES, Lalouel JM, Leppert M. Hoehe MR, et al. Among authors: stauffer d. Hum Mol Genet. 1992 Jun;1(3):175-8. doi: 10.1093/hmg/1.3.175. Hum Mol Genet. 1992. PMID: 1303174

3

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

Leppert M, Anderson VE, Quattlebaum T, Stauffer D, O'Connell P, Nakamura Y, Lalouel JM, White R. Leppert M, et al. Among authors: stauffer d. Nature. 1989 Feb 16;337(6208):647-8. doi: 10.1038/337647a0. Nature. 1989. PMID: 2918897

4

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

Lewis RA, Otterud B, Stauffer D, Lalouel JM, Leppert M. Lewis RA, et al. Among authors: stauffer d. Genomics. 1990 Jun;7(2):250-6. doi: 10.1016/0888-7543(90)90547-8. Genomics. 1990. PMID: 1971808

5

A genetic linkage map with 29 loci spanning human chromosome 13q.

Gerken S, Leppert M, O'Connell P, Cavenee W, James CD, Ballard L, Stauffer D, Elsner T, Plaetke R, Lalouel JM, et al. Gerken S, et al. Among authors: stauffer d. Genomics. 1993 May;16(2):515-9. doi: 10.1006/geno.1993.1219. Genomics. 1993. PMID: 8100218

6

The gene for familial polyposis coli maps to the long arm of chromosome 5.

Leppert M, Dobbs M, Scambler P, O'Connell P, Nakamura Y, Stauffer D, Woodward S, Burt R, Hughes J, Gardner E, et al. Leppert M, et al. Among authors: stauffer d. Science. 1987 Dec 4;238(4832):1411-3. doi: 10.1126/science.3479843. Science. 1987. PMID: 3479843

7

Discordance of T-cell receptor beta-chain genes in familial multiple sclerosis.

Lynch SG, Rose JW, Petajan JH, Stauffer D, Kamerath C, Leppert M. Lynch SG, et al. Among authors: stauffer d. Ann Neurol. 1991 Sep;30(3):402-10. doi: 10.1002/ana.410300313. Ann Neurol. 1991. PMID: 1683213

8

D7S449 detects a HindIII polymorphism tightly linked to the MET gene on chromosome 7.

Dean M, Stewart C, Perry A, Stauffer D, Otterud B, White R, Leppert M. Dean M, et al. Among authors: stauffer d. Nucleic Acids Res. 1990 Dec 11;18(23):7199. doi: 10.1093/nar/18.23.7199-a. Nucleic Acids Res. 1990. PMID: 1979868 Free PMC article. No abstract available.

9

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.

Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR. Allikmets R, et al. Among authors: stauffer d. Nat Genet. 1997 Mar;15(3):236-46. doi: 10.1038/ng0397-236. Nat Genet. 1997. PMID: 9054934

10

D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7.

Dean M, Stewart C, Perry A, Stauffer D, Otterud B, White R, Leppert M. Dean M, et al. Among authors: stauffer d. Nucleic Acids Res. 1991 Jan 11;19(1):200. doi: 10.1093/nar/19.1.200-a. Nucleic Acids Res. 1991. PMID: 1672750 Free PMC article. No abstract available.

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