Bingham EL - Search Results

1

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: bingham el. Hum Hered. 1995 Jul-Aug;45(4):206-10. doi: 10.1159/000154290. Hum Hered. 1995. PMID: 7558052

2

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. Am J Hum Genet. 1996 Jul;59(1):152-8. Am J Hum Genet. 1996. PMID: 8659520 Free PMC article.

3

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. Among authors: bingham el. Am J Hum Genet. 1990 Oct;47(4):616-21. Am J Hum Genet. 1990. PMID: 1977307 Free PMC article.

4

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: bingham el. Hum Hered. 1996 Jul-Aug;46(4):211-20. doi: 10.1159/000154356. Hum Hered. 1996. PMID: 8807324

5

X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC.

Pawar H, Bingham EL, Hiriyanna K, Segal M, Richards JE, Sieving PA. Pawar H, et al. Among authors: bingham el. Hum Hered. 1996 Nov-Dec;46(6):329-35. doi: 10.1159/000154373. Hum Hered. 1996. PMID: 8956029

6

Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave.

Sieving PA, Bingham EL, Kemp J, Richards J, Hiriyanna K. Sieving PA, et al. Among authors: bingham el. Am J Ophthalmol. 1999 Aug;128(2):179-84. doi: 10.1016/s0002-9394(99)00144-0. Am J Ophthalmol. 1999. PMID: 10458173

7

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.

Hiriyanna KT, Bingham EL, Yashar BM, Ayyagari R, Fishman G, Small KW, Weinberg DV, Weleber RG, Lewis RA, Andreasson S, Richards JE, Sieving PA. Hiriyanna KT, et al. Among authors: bingham el. Hum Mutat. 1999;14(5):423-7. doi: 10.1002/(SICI)1098-1004(199911)14:5<423::AID-HUMU8>3.0.CO;2-D. Hum Mutat. 1999. PMID: 10533068 Free article.

8

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: bingham el. Genomics. 2002 Aug;80(2):166-71. doi: 10.1006/geno.2002.6815. Genomics. 2002. PMID: 12160730

9

Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation.

Sieving PA, Boskovich S, Bingham E, Pawar H. Sieving PA, et al. Trans Am Ophthalmol Soc. 1996;94:275-94; discussion 295-7. Trans Am Ophthalmol Soc. 1996. PMID: 8981701 Free PMC article.

10

Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene.

Ayyagari R, Griesinger IB, Bingham E, Lark KK, Moroi SE, Sieving PA. Ayyagari R, et al. Arch Ophthalmol. 2000 Jan;118(1):85-92. doi: 10.1001/archopht.118.1.85. Arch Ophthalmol. 2000. PMID: 10636420

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