Bruns GA - Search Results

1

(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein.

Khurana TS, Engle EC, Bennett RR, Silverman GA, Selig S, Bruns GA, Kunkel LM. Khurana TS, et al. Among authors: bruns ga. Hum Mol Genet. 1994 May;3(5):841. doi: 10.1093/hmg/3.5.841-a. Hum Mol Genet. 1994. PMID: 8081380 No abstract available.

2

Reassignment of pEFD70.3 (D18S23) to human chromosome band 21q22.2 (D21S412) by physical mapping.

Silverman GA, Jenkins R, Bruns GA, LeBeau MM. Silverman GA, et al. Among authors: bruns ga. Hum Mol Genet. 1993 Mar;2(3):331. doi: 10.1093/hmg/2.3.331. Hum Mol Genet. 1993. PMID: 8499926 No abstract available.

3

pMCT108.2 is a chimaeric clone which physically maps to human chromosome bands 9q33 (D9S203) and 18q21.1 (D18S24).

Lia KM, Bruns GA, LeBeau MM, Silverman GA. Lia KM, et al. Among authors: bruns ga. Hum Mol Genet. 1993 Mar;2(3):332. doi: 10.1093/hmg/2.3.332. Hum Mol Genet. 1993. PMID: 8499927 No abstract available.

4

Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11.

Beggs AH, Byers TJ, Knoll JH, Boyce FM, Bruns GA, Kunkel LM. Beggs AH, et al. Among authors: bruns ga. J Biol Chem. 1992 May 5;267(13):9281-8. J Biol Chem. 1992. PMID: 1339456 Free article.

5

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.

Fontaine B, Khurana TS, Hoffman EP, Bruns GA, Haines JL, Trofatter JA, Hanson MP, Rich J, McFarlane H, Yasek DM, et al. Fontaine B, et al. Among authors: bruns ga. Science. 1990 Nov 16;250(4983):1000-2. doi: 10.1126/science.2173143. Science. 1990. PMID: 2173143

6

Two RFLPs identified by a human chromosome #2 clone at 2p15-2p16 (HGM8 assignment no. D2S5).

Shiloh Y, Kanda N, Kunkel LM, Bruns G, Sakai K, Latt SA. Shiloh Y, et al. Nucleic Acids Res. 1985 Jul 25;13(14):5403. doi: 10.1093/nar/13.14.5403. Nucleic Acids Res. 1985. PMID: 4022784 Free PMC article. No abstract available.

7

Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

de Martinville B, Kunkel LM, Bruns G, Morlé F, Koenig M, Mandel JL, Horwich A, Latt SA, Gusella JF, Housman D, et al. de Martinville B, et al. Am J Hum Genet. 1985 Mar;37(2):235-49. Am J Hum Genet. 1985. PMID: 2984924 Free PMC article.

8

Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.

Harris P, Lalande M, Stroh H, Bruns G, Flint A, Latt SA. Harris P, et al. Hum Genet. 1987 Oct;77(2):95-103. doi: 10.1007/BF00272372. Hum Genet. 1987. PMID: 2888723

9

A strategy to reveal high-frequency RFLPs along the human X chromosome.

Aldridge J, Kunkel L, Bruns G, Tantravahi U, Lalande M, Brewster T, Moreau E, Wilson M, Bromley W, Roderick T, et al. Aldridge J, et al. Am J Hum Genet. 1984 May;36(3):546-64. Am J Hum Genet. 1984. PMID: 6328976 Free PMC article.

10

A deletion map of the WAGR region on chromosome 11.

Gessler M, Thomas GH, Couillin P, Junien C, McGillivray BC, Hayden M, Jaschek G, Bruns GA. Gessler M, et al. Among authors: bruns ga. Am J Hum Genet. 1989 Apr;44(4):486-95. Am J Hum Genet. 1989. PMID: 2539014 Free PMC article.

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