Sieving PA - Search Results

1

X-linked recessive atrophic macular degeneration from RPGR mutation.

Ayyagari R, Demirci FY, Liu J, Bingham EL, Stringham H, Kakuk LE, Boehnke M, Gorin MB, Richards JE, Sieving PA. Ayyagari R, et al. Among authors: sieving pa. Genomics. 2002 Aug;80(2):166-71. doi: 10.1006/geno.2002.6815. Genomics. 2002. PMID: 12160730

2

Rhodopsin Thr58Arg mutation in a family with autosomal dominant retinitis pigmentosa.

Richards JE, Kuo CY, Boehnke M, Sieving PA. Richards JE, et al. Among authors: sieving pa. Ophthalmology. 1991 Dec;98(12):1797-805. doi: 10.1016/s0161-6420(91)32047-5. Ophthalmology. 1991. PMID: 1775313

3

Fenestrated sheen macular dystrophy.

Sneed SR, Sieving PA. Sneed SR, et al. Among authors: sieving pa. Am J Ophthalmol. 1991 Jul 15;112(1):1-7. doi: 10.1016/s0002-9394(14)76204-x. Am J Ophthalmol. 1991. PMID: 1882912

4

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.

Sieving PA, Bingham EL, Roth MS, Young MR, Boehnke M, Kuo CY, Ginsburg D. Sieving PA, et al. Am J Hum Genet. 1990 Oct;47(4):616-21. Am J Hum Genet. 1990. PMID: 1977307 Free PMC article.

5

Refined genetic mapping of juvenile X-linked retinoschisis.

Pawar H, Bingham EL, Lunetta KL, Segal M, Richards JE, Boehnke M, Sieving PA. Pawar H, et al. Among authors: sieving pa. Hum Hered. 1995 Jul-Aug;45(4):206-10. doi: 10.1159/000154290. Hum Hered. 1995. PMID: 7558052

6

Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa.

Richards JE, Scott KM, Sieving PA. Richards JE, et al. Among authors: sieving pa. Ophthalmology. 1995 Apr;102(4):669-77. doi: 10.1016/s0161-6420(95)30972-4. Ophthalmology. 1995. PMID: 7724183

7

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.

Sieving PA, Richards JE, Naarendorp F, Bingham EL, Scott K, Alpern M. Sieving PA, et al. Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):880-4. doi: 10.1073/pnas.92.3.880. Proc Natl Acad Sci U S A. 1995. PMID: 7846071 Free PMC article.

8

Dinucleotide repeat polymorphism at the DXS977 locus.

Yan D, Wong D, Zheng K, Thiselton D, Fujita R, Sieving PA, Bhattacharya SS, Yang-Feng TL, Richards JE, Swaroop A. Yan D, et al. Among authors: sieving pa. Hum Mol Genet. 1994 Jun;3(6):1030. doi: 10.1093/hmg/3.6.1030. Hum Mol Genet. 1994. PMID: 7951222 No abstract available.

9

A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Fujita R, Bingham E, Forsythe P, McHenry C, Aita V, Navia BA, Dry K, Segal M, Devoto M, Bruns G, Wright AF, Ott J, Sieving PA, Swaroop A. Fujita R, et al. Among authors: sieving pa. Am J Hum Genet. 1996 Jul;59(1):152-8. Am J Hum Genet. 1996. PMID: 8659520 Free PMC article.

10

Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.

Hou YC, Richards JE, Bingham EL, Pawar H, Scott K, Segal M, Lunetta KL, Boehnke M, Sieving PA. Hou YC, et al. Among authors: sieving pa. Hum Hered. 1996 Jul-Aug;46(4):211-20. doi: 10.1159/000154356. Hum Hered. 1996. PMID: 8807324

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