Sunden SL - Search Results

1

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25).

Héon E, Sheth BP, Kalenak JW, Sunden SL, Streb LM, Taylor CM, Alward WL, Sheffield VC, Stone EM. Héon E, et al. Among authors: sunden sl. Hum Mol Genet. 1995 Aug;4(8):1435-9. doi: 10.1093/hmg/4.8.1435. Hum Mol Genet. 1995. PMID: 7581385

2

Linkage of posterior polymorphous corneal dystrophy to 20q11.

Héon E, Mathers WD, Alward WL, Weisenthal RW, Sunden SL, Fishbaugh JA, Taylor CM, Krachmer JH, Sheffield VC, Stone EM. Héon E, et al. Among authors: sunden sl. Hum Mol Genet. 1995 Mar;4(3):485-8. doi: 10.1093/hmg/4.3.485. Hum Mol Genet. 1995. PMID: 7795607

3

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping.

Sheffield VC, Carmi R, Kwitek-Black A, Rokhlina T, Nishimura D, Duyk GM, Elbedour K, Sunden SL, Stone EM. Sheffield VC, et al. Among authors: sunden sl. Hum Mol Genet. 1994 Aug;3(8):1331-5. doi: 10.1093/hmg/3.8.1331. Hum Mol Genet. 1994. PMID: 7987310

4

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps.

Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, et al. Sheffield VC, et al. Among authors: sunden sl. Hum Mol Genet. 1995 Oct;4(10):1837-44. doi: 10.1093/hmg/4.10.1837. Hum Mol Genet. 1995. PMID: 8595404

5

Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes.

Sunden SL, Alward WL, Nichols BE, Rokhlina TR, Nystuen A, Stone EM, Sheffield VC. Sunden SL, et al. Genome Res. 1996 Sep;6(9):862-9. doi: 10.1101/gr.6.9.862. Genome Res. 1996. PMID: 8889553 Free article.

6

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).

Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J, Sheffield VC, Sunden S, Duyk GM, et al. Murray JC, et al. Science. 1994 Sep 30;265(5181):2049-54. doi: 10.1126/science.8091227. Science. 1994. PMID: 8091227

7

Identification of a gene that causes primary open angle glaucoma.

Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Stone EM, et al. Among authors: sunden sl. Science. 1997 Jan 31;275(5300):668-70. doi: 10.1126/science.275.5300.668. Science. 1997. PMID: 9005853

8

Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2.

Sunden SL, Businga T, Beck J, McClain A, Gastier JM, Pulido JC, Yandava CN, Brody T, Ghazizadeh J, Weber JL, Duyk GM, Murray JC, Buetow KH, Sheffield VC. Sunden SL, et al. Genomics. 1996 Feb 15;32(1):15-20. doi: 10.1006/geno.1996.0071. Genomics. 1996. PMID: 8786107

9

Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers.

Gastier JM, Pulido JC, Sunden S, Brody T, Buetow KH, Murray JC, Weber JL, Hudson TJ, Sheffield VC, Duyk GM. Gastier JM, et al. Hum Mol Genet. 1995 Oct;4(10):1829-36. doi: 10.1093/hmg/4.10.1829. Hum Mol Genet. 1995. PMID: 8595403

10

Development of a screening set for new (CAG/CTG)n dynamic mutations.

Gastier JM, Brody T, Pulido JC, Businga T, Sunden S, Hu X, Maitra S, Buetow KH, Murray JC, Sheffield VC, Boguski M, Duyk GM, Hudson TJ. Gastier JM, et al. Genomics. 1996 Feb 15;32(1):75-85. doi: 10.1006/geno.1996.0078. Genomics. 1996. PMID: 8786123

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