Klintworth GK - Search Results

1

Linkage of a gene for macular corneal dystrophy to chromosome 16.

Vance JM, Jonasson F, Lennon F, Sarrica J, Damji KF, Stauffer J, Pericak-Vance MA, Klintworth GK. Vance JM, et al. Among authors: klintworth gk. Am J Hum Genet. 1996 Apr;58(4):757-62. Am J Hum Genet. 1996. PMID: 8644739 Free PMC article.

2

Different mutations in carbohydrate sulfotransferase 6 (CHST6) gene cause macular corneal dystrophy types I and II in a single sibship.

Liu NP, Bao W, Smith CF, Vance JM, Klintworth GK. Liu NP, et al. Among authors: klintworth gk. Am J Ophthalmol. 2005 Jun;139(6):1118-20. doi: 10.1016/j.ajo.2004.11.054. Am J Ophthalmol. 2005. PMID: 15953452

3

Coexistence of macular corneal dystrophy types I and II in a single sibship.

Liu NP, Baldwin J, Lennon F, Stajich JM, Thonar EJ, Pericak-Vance MA, Klintworth GK, Vance JM. Liu NP, et al. Among authors: klintworth gk. Br J Ophthalmol. 1998 Mar;82(3):241-4. doi: 10.1136/bjo.82.3.241. Br J Ophthalmol. 1998. PMID: 9602619 Free PMC article.

4

Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I gene.

Liu NP, Baldwin J, Jonasson F, Dew-Knight S, Stajich JM, Lennon F, Pericak-Vance MA, Klintworth GK, Vance JM. Liu NP, et al. Among authors: klintworth gk. Am J Hum Genet. 1998 Sep;63(3):912-7. doi: 10.1086/302001. Am J Hum Genet. 1998. PMID: 9718332 Free PMC article. No abstract available.

5

Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.

Liu NP, Dew-Knight S, Jonasson F, Gilbert JR, Klintworth GK, Vance JM. Liu NP, et al. Among authors: klintworth gk. Mol Vis. 2000 Jun 19;6:95-100. Mol Vis. 2000. PMID: 10869098 Free article.

6

Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.

Liu NP, Dew-Knight S, Rayner M, Jonasson F, Akama TO, Fukuda MN, Bao W, Gilbert JR, Vance JM, Klintworth GK. Liu NP, et al. Among authors: klintworth gk. Mol Vis. 2000 Dec 13;6:261-4. Mol Vis. 2000. PMID: 11139648 Free article.

7

A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis.

Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM. Allingham RR, et al. Among authors: klintworth gk. Am J Hum Genet. 2001 Feb;68(2):491-4. doi: 10.1086/318194. Epub 2001 Jan 16. Am J Hum Genet. 2001. PMID: 11170897 Free PMC article.

8

Genome-wide linkage scan in fuchs endothelial corneal dystrophy.

Afshari NA, Li YJ, Pericak-Vance MA, Gregory S, Klintworth GK. Afshari NA, et al. Among authors: klintworth gk. Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1093-7. doi: 10.1167/iovs.08-1839. Epub 2008 May 23. Invest Ophthalmol Vis Sci. 2009. PMID: 18502986 Free PMC article.

9

Macular corneal dystrophy in Iceland. A clinical, genealogic, and immunohistochemical study of 28 patients.

Jonasson F, Oshima E, Thonar EJ, Smith CF, Johannsson JH, Klintworth GK. Jonasson F, et al. Among authors: klintworth gk. Ophthalmology. 1996 Jul;103(7):1111-7. doi: 10.1016/s0161-6420(96)30559-9. Ophthalmology. 1996. PMID: 8684802

10

Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland.

Liu NP, Smith CF, Bowling BL, Jonasson F, Klintworth GK. Liu NP, et al. Among authors: klintworth gk. Mol Vis. 2006 Oct 2;12:1148-52. Mol Vis. 2006. PMID: 17093400 Free article.

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