Wirtz MK - Search Results

1

Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusen.

Edwards AO, Klein ML, Berselli CB, Hejtmancik JF, Rust K, Wirtz MK, Weleber RG, Acott TS. Edwards AO, et al. Among authors: wirtz mk. Am J Ophthalmol. 1998 Sep;126(3):417-24. doi: 10.1016/s0002-9394(98)00097-x. Am J Ophthalmol. 1998. PMID: 9744375

2

Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q.

Klein ML, Schultz DW, Edwards A, Matise TC, Rust K, Berselli CB, Trzupek K, Weleber RG, Ott J, Wirtz MK, Acott TS. Klein ML, et al. Among authors: wirtz mk. Arch Ophthalmol. 1998 Aug;116(8):1082-8. doi: 10.1001/archopht.116.8.1082. Arch Ophthalmol. 1998. PMID: 9715689

3

Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.

Wirtz MK, Samples JR, Kramer PL, Rust K, Yount J, Acott TS, Koler RD, Cisler J, Jahed A, Gorlin RJ, Godfrey M. Wirtz MK, et al. Am J Med Genet. 1996 Oct 2;65(1):68-75. doi: 10.1002/(SICI)1096-8628(19961002)65:1<68::AID-AJMG11>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8914744

4

Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.

Wirtz MK, Samples JR, Kramer PL, Rust K, Topinka JR, Yount J, Koler RD, Acott TS. Wirtz MK, et al. Am J Hum Genet. 1997 Feb;60(2):296-304. Am J Hum Genet. 1997. PMID: 9012402 Free PMC article.

5

GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36.

Wirtz MK, Samples JR, Rust K, Lie J, Nordling L, Schilling K, Acott TS, Kramer PL. Wirtz MK, et al. Arch Ophthalmol. 1999 Feb;117(2):237-41. doi: 10.1001/archopht.117.2.237. Arch Ophthalmol. 1999. PMID: 10037570

6

Discrete expression and distribution pattern of TIMP-3 in the human retina and choroid.

Vranka JA, Johnson E, Zhu X, Shepardson A, Alexander JP, Bradley JM, Wirtz MK, Weleber RG, Klein ML, Acott TS. Vranka JA, et al. Among authors: wirtz mk. Curr Eye Res. 1997 Feb;16(2):102-10. doi: 10.1076/ceyr.16.2.102.5086. Curr Eye Res. 1997. PMID: 9068940

7

Expression profile and genome location of cDNA clones from an infant human trabecular meshwork cell library.

Wirtz MK, Samples JR, Xu H, Severson T, Acott TS. Wirtz MK, et al. Invest Ophthalmol Vis Sci. 2002 Dec;43(12):3698-704. Invest Ophthalmol Vis Sci. 2002. PMID: 12454039

8

Prospects for genetic intervention in primary open-angle glaucoma.

Wirtz MK, Acott TS, Samples JR, Morrison JC. Wirtz MK, et al. Drugs Aging. 1998 Nov;13(5):333-40. doi: 10.2165/00002512-199813050-00001. Drugs Aging. 1998. PMID: 9829162 Review.

9

Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis.

Samples JR, Kitsos G, Economou-Petersen E, Steinkamp P, Sykes R, Rust K, Patzer C, Grigoriadou M, Aperis G, Psilas K, Petersen MB, Wirtz MK. Samples JR, et al. Among authors: wirtz mk. Clin Genet. 2004 Jan;65(1):40-4. doi: 10.1111/j..2004.00182.x. Clin Genet. 2004. PMID: 15032973

10

A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability.

Petersen MB, Kitsos G, Samples JR, Gaudette ND, Economou-Petersen E, Sykes R, Rust K, Grigoriadou M, Aperis G, Choi D, Psilas K, Craig JE, Kramer PL, Mackey DA, Wirtz MK. Petersen MB, et al. Among authors: wirtz mk. Invest Ophthalmol Vis Sci. 2006 Feb;47(2):620-5. doi: 10.1167/iovs.05-0631. Invest Ophthalmol Vis Sci. 2006. PMID: 16431959

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