Hogan K - Search Results

1

Linkage mapping of the human gene for the alpha 1 subunit of the cardiac DHP-sensitive Ca2+ channel (CACNL1A1) to chromosome 12p13.2-pter using a dinucleotide repeat.

Powers PA, Gregg RG, Hogan K. Powers PA, et al. Among authors: hogan k. Genomics. 1992 Sep;14(1):206-7. doi: 10.1016/s0888-7543(05)80312-x. Genomics. 1992. PMID: 1330882 No abstract available.

2

Dinucleotide repeat polymorphism at the D10S178 locus.

Couch FJ, Gregg RG, McCarthy TV, Hogan K. Couch FJ, et al. Among authors: hogan k. Nucleic Acids Res. 1992 Mar 25;20(6):1431. Nucleic Acids Res. 1992. PMID: 1561111 Free PMC article. No abstract available.

3

Dinucleotide repeat polymorphism at the D10S179 locus.

Couch FJ, McCarthy TV, Hogan K, Gregg RG. Couch FJ, et al. Among authors: hogan k. Nucleic Acids Res. 1992 Mar 25;20(6):1431. Nucleic Acids Res. 1992. PMID: 1561112 Free PMC article. No abstract available.

4

Assignment of the human gene for the alpha 1 subunit of the cardiac DHP-sensitive Ca2+ channel (CCHL1A1) to chromosome 12p12-pter.

Powers PA, Gregg RG, Lalley PA, Liao M, Hogan K. Powers PA, et al. Among authors: hogan k. Genomics. 1991 Jul;10(3):835-9. doi: 10.1016/0888-7543(91)90471-p. Genomics. 1991. PMID: 1653763

5

Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter.

Gregg RG, Metzenberg AB, Hogan K, Sekhon G, Laxova R. Gregg RG, et al. Among authors: hogan k. Genomics. 1991 Apr;9(4):701-6. doi: 10.1016/0888-7543(91)90363-j. Genomics. 1991. PMID: 1674730

6

Dinucleotide repeat polymorphism at the D17S518 locus.

Couch FJ, McCarthy TV, Gregg RG, Hogan K. Couch FJ, et al. Among authors: hogan k. Nucleic Acids Res. 1991 Sep 25;19(18):5093. Nucleic Acids Res. 1991. PMID: 1923789 Free PMC article. No abstract available.

7

Dinucleotide repeat polymorphism at the D8S161 locus.

Couch FJ, McCarthy TV, Gregg RG, Hogan K. Couch FJ, et al. Among authors: hogan k. Nucleic Acids Res. 1991 Sep 25;19(18):5093. Nucleic Acids Res. 1991. PMID: 1923790 Free PMC article. No abstract available.

8

Cloning of the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3).

Hogan K, Powers PA, Gregg RG. Hogan K, et al. Genomics. 1994 Dec;24(3):608-9. doi: 10.1006/geno.1994.1677. Genomics. 1994. PMID: 7713519 No abstract available.

9

Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32.

Gregg RG, Couch F, Hogan K, Powers PA. Gregg RG, et al. Among authors: hogan k. Genomics. 1993 Jan;15(1):107-12. doi: 10.1006/geno.1993.1017. Genomics. 1993. PMID: 7916735

10

Localization of the gene encoding the alpha 2/delta subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21-q22 by somatic cell hybrid analysis.

Powers PA, Scherer SW, Tsui LC, Gregg RG, Hogan K. Powers PA, et al. Among authors: hogan k. Genomics. 1994 Jan 1;19(1):192-3. doi: 10.1006/geno.1994.1044. Genomics. 1994. PMID: 8188232 No abstract available.

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