Daiger SP - Search Results

1

Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites.

Sohocki MM, Sullivan LS, Harrison WR, Sodergren EJ, Elder FF, Weinstock G, Tanase S, Daiger SP. Sohocki MM, et al. Among authors: daiger sp. Genomics. 1997 Mar 1;40(2):247-52. doi: 10.1006/geno.1996.4604. Genomics. 1997. PMID: 9119391

2

Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24.

Yee RW, Sullivan LS, Lai HT, Stock EL, Lu Y, Khan MN, Blanton SH, Daiger SP. Yee RW, et al. Among authors: daiger sp. Genomics. 1997 Nov 15;46(1):152-4. doi: 10.1006/geno.1997.5028. Genomics. 1997. PMID: 9403072

3

Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disorders.

Sohocki MM, Malone KA, Sullivan LS, Daiger SP. Sohocki MM, et al. Among authors: daiger sp. Genomics. 1999 May 15;58(1):29-33. doi: 10.1006/geno.1999.5810. Genomics. 1999. PMID: 10331942

4

Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.

Bowne SJ, Daiger SP, Malone KA, Heckenlively JR, Kennan A, Humphries P, Hughbanks-Wheaton D, Birch DG, Liu Q, Pierce EA, Zuo J, Huang Q, Donovan DD, Sullivan LS. Bowne SJ, et al. Among authors: daiger sp. Mol Vis. 2003 Apr 24;9:129-37. Mol Vis. 2003. PMID: 12724644 Free PMC article.

5

Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25.

Sullivan LS, Zhao X, Bowne SJ, Xu X, Daiger SP, Yee SB, Yee RW. Sullivan LS, et al. Among authors: daiger sp. Curr Eye Res. 2003 Oct;27(4):223-6. doi: 10.1076/ceyr.27.4.223.16595. Curr Eye Res. 2003. PMID: 14562173

6

A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement.

Bowne SJ, Humphries MM, Sullivan LS, Kenna PF, Tam LC, Kiang AS, Campbell M, Weinstock GM, Koboldt DC, Ding L, Fulton RS, Sodergren EJ, Allman D, Millington-Ward S, Palfi A, McKee A, Blanton SH, Slifer S, Konidari I, Farrar GJ, Daiger SP, Humphries P. Bowne SJ, et al. Among authors: daiger sp. Eur J Hum Genet. 2011 Oct;19(10):1074-81. doi: 10.1038/ejhg.2011.86. Epub 2011 Jun 8. Eur J Hum Genet. 2011. PMID: 21654732 Free PMC article.

7

X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

McGuire RE, Sullivan LS, Blanton SH, Church MW, Heckenlively JR, Daiger SP. McGuire RE, et al. Among authors: daiger sp. Am J Hum Genet. 1995 Jul;57(1):87-94. Am J Hum Genet. 1995. PMID: 7611300 Free PMC article.

8

Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family.

McGuire RE, Gannon AM, Sullivan LS, Rodriguez JA, Daiger SP. McGuire RE, et al. Among authors: daiger sp. Hum Genet. 1995 Jan;95(1):71-4. doi: 10.1007/BF00225078. Hum Genet. 1995. PMID: 7814030

9

Inherited retinal degeneration: exceptional genetic and clinical heterogeneity.

Sullivan LS, Daiger SP. Sullivan LS, et al. Among authors: daiger sp. Mol Med Today. 1996 Sep;2(9):380-6. doi: 10.1016/s1357-4310(96)10037-x. Mol Med Today. 1996. PMID: 8885257 Review.

10

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.

Sohocki MM, Sullivan LS, Mintz-Hittner HA, Birch D, Heckenlively JR, Freund CL, McInnes RR, Daiger SP. Sohocki MM, et al. Among authors: daiger sp. Am J Hum Genet. 1998 Nov;63(5):1307-15. doi: 10.1086/302101. Am J Hum Genet. 1998. PMID: 9792858 Free PMC article.

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