Leach RJ - Search Results

1

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M. Singh NA, et al. Among authors: leach rj. Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25. Nat Genet. 1998. PMID: 9425895

2

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p.

Whitney M, Thayer M, Reifsteck C, Olson S, Smith L, Jakobs PM, Leach R, Naylor S, Joenje H, Grompe M. Whitney M, et al. Nat Genet. 1995 Nov;11(3):341-3. doi: 10.1038/ng1195-341. Nat Genet. 1995. PMID: 7581463

3

New variants of the human and rat nuclear hormone receptor, TR4: expression and chromosomal localization of the human gene.

Yoshikawa T, DuPont BR, Leach RJ, Detera-Wadleigh SD. Yoshikawa T, et al. Among authors: leach rj. Genomics. 1996 Jul 15;35(2):361-6. doi: 10.1006/geno.1996.0368. Genomics. 1996. PMID: 8661150

4

Localization of a gene for a glutamate binding subunit of a NMDA receptor (GRINA) to 8q24.

Lewis TB, Wood S, Michaelis EK, DuPont BR, Leach RJ. Lewis TB, et al. Among authors: leach rj. Genomics. 1996 Feb 15;32(1):131-3. doi: 10.1006/geno.1996.0088. Genomics. 1996. PMID: 8786101

5

Assignment of the human nuclear hormone receptor, NUC1 (PPARD), to chromosome 6p21.1-p21.2.

Yoshikawa T, Brkanac Z, Dupont BR, Xing GQ, Leach RJ, Detera-Wadleigh SD. Yoshikawa T, et al. Among authors: leach rj. Genomics. 1996 Aug 1;35(3):637-8. doi: 10.1006/geno.1996.0417. Genomics. 1996. PMID: 8812511 No abstract available.

6

Assignment of matrix metalloproteinase 9 (Mmp9) to mouse chromosome 2 bands H1-H2.

DuPont BR, Linn R, Knight CB, Roodman GD, Sakaguchi AY, Lalley PA, Fournier RE, Leach RJ. DuPont BR, et al. Among authors: leach rj. Cytogenet Cell Genet. 1996;74(1-2):118-9. doi: 10.1159/000134396. Cytogenet Cell Genet. 1996. PMID: 8893816 No abstract available.

7

Assignment of DMP1 to human chromosome 4 band q21 by in situ hybridization.

MacDougall M, DuPont BR, Simmons D, Leach RJ. MacDougall M, et al. Among authors: leach rj. Cytogenet Cell Genet. 1996;74(3):189. doi: 10.1159/000134410. Cytogenet Cell Genet. 1996. PMID: 8941370 No abstract available.

8

Reassignment of the 92-kDa type IV collagenase gene (CLG4B) to human chromosome 20.

Linn R, DuPont BR, Knight CB, Plaetke R, Leach RJ. Linn R, et al. Among authors: leach rj. Cytogenet Cell Genet. 1996;72(2-3):159-61. doi: 10.1159/000134175. Cytogenet Cell Genet. 1996. PMID: 8978762

9

Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.

Gay CT, Hardies LJ, Rauch RA, Lancaster JL, Plaetke R, DuPont BR, Cody JD, Cornell JE, Herndon RC, Ghidoni PD, Schiff JM, Kaye CI, Leach RJ, Fox PT. Gay CT, et al. Among authors: leach rj. Am J Med Genet. 1997 Jul 25;74(4):422-31. doi: 10.1002/(sici)1096-8628(19970725)74:4<422::aid-ajmg14>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9259379

10

Genetic linkage of Paget disease of the bone to chromosome 18q.

Cody JD, Singer FR, Roodman GD, Otterund B, Lewis TB, Leppert M, Leach RJ. Cody JD, et al. Among authors: leach rj. Am J Hum Genet. 1997 Nov;61(5):1117-22. doi: 10.1086/301601. Am J Hum Genet. 1997. PMID: 9345096 Free PMC article.

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