Otterud B - Search Results

1

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: otterud b. 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.

2

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: otterud b. 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.

3

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: otterud b. Hum Mol Genet. 1992 Jun;1(3):175-8. doi: 10.1093/hmg/1.3.175. Hum Mol Genet. 1992. PMID: 1303174

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: otterud b. Genomics. 1990 Jun;7(2):250-6. doi: 10.1016/0888-7543(90)90547-8. Genomics. 1990. PMID: 1971808

5

The human endothelin-1 gene (EDN1) encoding a peptide with potent vasoactive properties maps distal to HLA on chromosome arm 6p in close linkage to D6S89.

Hoehe MR, Ehrenreich H, Otterud B, Caenazzo L, Plaetke R, Zander H, Leppert M. Hoehe MR, et al. Among authors: otterud b. Cytogenet Cell Genet. 1993;62(2-3):131-5. doi: 10.1159/000133455. Cytogenet Cell Genet. 1993. PMID: 8428511

6

Hereditary spastic paraplegia linked to chromosome 15q: Analysis of candidate genes.

Fink JK, Jones SM, Sharp GB, Lange BM, Otterud B, Leppert M. Fink JK, et al. Among authors: otterud b. Neurology. 1996 Mar;46(3):835-6. doi: 10.1212/wnl.46.3.835. Neurology. 1996. PMID: 8618696

7

Description of a second microsatellite marker and linkage analysis of the muscle glycogen synthase locus in familial NIDDM.

Elbein SC, Hoffman M, Ridinger D, Otterud B, Leppert M. Elbein SC, et al. Among authors: otterud b. Diabetes. 1994 Aug;43(8):1061-5. doi: 10.2337/diab.43.8.1061. Diabetes. 1994. PMID: 7913686

8

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.

Heath H 3rd, Jackson CE, Otterud B, Leppert MF. Heath H 3rd, et al. Among authors: otterud b. Am J Hum Genet. 1993 Jul;53(1):193-200. Am J Hum Genet. 1993. PMID: 8317484 Free PMC article.

9

Genetic mapping of adrenergic receptor genes in humans.

Hoehe MR, Otterud B, Hsieh WT, Martinez MM, Stauffer D, Holik J, Berrettini WH, Byerley WF, Gershon ES, Lalouel JM, et al. Hoehe MR, et al. Among authors: otterud b. J Mol Med (Berl). 1995 Jun;73(6):299-306. doi: 10.1007/BF00231616. J Mol Med (Berl). 1995. PMID: 7583452

10

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

Leppert M, Baird L, Anderson KL, Otterud B, Lupski JR, Lewis RA. Leppert M, et al. Among authors: otterud b. Nat Genet. 1994 May;7(1):108-12. doi: 10.1038/ng0594-108. Nat Genet. 1994. PMID: 8075632

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