Stauffer D - Search Results

1

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

2

Physical and genetic localization of a Shab subfamily potassium channel (KCNB1) gene to chromosomal region 20q13.2.

Melis R, Stauffer D, Zhao X, Zhu XL, Albrecht B, Pongs O, Brothman A, Leppert M. Melis R, et al. Among authors: stauffer d. Genomics. 1995 Jan 1;25(1):285-7. doi: 10.1016/0888-7543(95)80138-c. Genomics. 1995. PMID: 7774931

3

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

4

Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy.

Flanigan KM, Coffeen CM, Sexton L, Stauffer D, Brunner S, Leppert MF. Flanigan KM, et al. Among authors: stauffer d. Neuromuscul Disord. 2001 Sep;11(6-7):525-9. doi: 10.1016/s0960-8966(01)00201-2. Neuromuscul Disord. 2001. PMID: 11525880

5

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.

6

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

7

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

8

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

9

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

10

Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.

Spirio L, Otterud B, Stauffer D, Lynch H, Lynch P, Watson P, Lanspa S, Smyrk T, Cavalieri J, Howard L, et al. Spirio L, et al. Among authors: stauffer d. Am J Hum Genet. 1992 Jul;51(1):92-100. Am J Hum Genet. 1992. PMID: 1319115 Free PMC article.

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