Shiang R - Search Results

1

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.

Buetow KH, Shiang R, Yang P, Nakamura Y, Lathrop GM, White R, Wasmuth JJ, Wood S, Berdahl LD, Leysens NJ, et al. Buetow KH, et al. Among authors: shiang r. Am J Hum Genet. 1991 May;48(5):911-25. Am J Hum Genet. 1991. PMID: 1673289 Free PMC article.

2

Pairwise linkage analysis of 11 loci on human chromosome 4.

Murray JC, Buetow KH, Smith M, Carlock L, Chakravarti A, Ferrell RF, Gedamu L, Gilliam C, Shiang R, DeHaven CR. Murray JC, et al. Among authors: shiang r. Am J Hum Genet. 1988 Mar;42(3):490-7. Am J Hum Genet. 1988. PMID: 2894759 Free PMC article.

3

Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.

Ryan SG, Dixon MJ, Nigro MA, Kelts KA, Markand ON, Terry JC, Shiang R, Wasmuth JJ, O'Connell P. Ryan SG, et al. Among authors: shiang r. Am J Hum Genet. 1992 Dec;51(6):1334-43. Am J Hum Genet. 1992. PMID: 1334371 Free PMC article.

4

Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci.

Murray JC, Shiang R, Carlock LR, Smith M, Buetow KH. Murray JC, et al. Among authors: shiang r. Hum Genet. 1987 Jul;76(3):274-7. doi: 10.1007/BF00283622. Hum Genet. 1987. PMID: 2885257

5

Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO).

Shiang R, Lidral AC, Ardinger HH, Buetow KH, Romitti PA, Munger RG, Murray JC. Shiang R, et al. Am J Hum Genet. 1993 Oct;53(4):836-43. Am J Hum Genet. 1993. PMID: 8105683 Free PMC article.

6

Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene.

Theilmann J, Kanani S, Shiang R, Robbins C, Quarrell O, Huggins M, Hedrick A, Weber B, Collins C, Wasmuth JJ, et al. Theilmann J, et al. Among authors: shiang r. J Med Genet. 1989 Nov;26(11):676-81. doi: 10.1136/jmg.26.11.676. J Med Genet. 1989. PMID: 2531224 Free PMC article.

7

Mapping of the human complement factor I gene to 4q25.

Shiang R, Murray JC, Morton CC, Buetow KH, Wasmuth JJ, Olney AH, Sanger WG, Goldberger G. Shiang R, et al. Genomics. 1989 Jan;4(1):82-6. doi: 10.1016/0888-7543(89)90318-2. Genomics. 1989. PMID: 2563353

8

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia.

Shiang R, Ryan SG, Zhu YZ, Hahn AF, O'Connell P, Wasmuth JJ. Shiang R, et al. Nat Genet. 1993 Dec;5(4):351-8. doi: 10.1038/ng1293-351. Nat Genet. 1993. PMID: 8298642

9

Generation of variability at VNTR loci in human DNA.

Wolff R, Nakamura Y, Odelberg S, Shiang R, White R. Wolff R, et al. Among authors: shiang r. EXS. 1991;58:20-38. doi: 10.1007/978-3-0348-7312-3_2. EXS. 1991. PMID: 1678356 Review.

10

Genes encoding adrenergic receptors are not clustered on the long arm of human chromosome 5.

Loftus SK, Shiang R, Warrington JA, Bengtsson U, McPherson JD, Wasmuth JJ. Loftus SK, et al. Among authors: shiang r. Cytogenet Cell Genet. 1994;67(2):69-74. doi: 10.1159/000133802. Cytogenet Cell Genet. 1994. PMID: 8039425

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