Weber BH - Search Results

1

Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter.

Weber BH, Vogt G, Wolz W, Ives EJ, Ewing CC. Weber BH, et al. Nat Genet. 1994 Jun;7(2):158-61. doi: 10.1038/ng0694-158. Nat Genet. 1994. PMID: 7920634

2

X-linked juvenile retinoschisis (RS) maps between DXS987 and DXS443.

Weber BH, Janocha S, Vogt G, Sander S, Ewing CC, Roesch M, Gibson A. Weber BH, et al. Cytogenet Cell Genet. 1995;69(1-2):35-7. doi: 10.1159/000133932. Cytogenet Cell Genet. 1995. PMID: 7835082

3

Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy.

Weber BH, Vogt G, Pruett RC, Stöhr H, Felbor U. Weber BH, et al. Nat Genet. 1994 Dec;8(4):352-6. doi: 10.1038/ng1294-352. Nat Genet. 1994. PMID: 7894485

4

High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11.

Weber BH, Vogt G, Stöhr H, Sander S, Walker D, Jones C. Weber BH, et al. Am J Hum Genet. 1994 Dec;55(6):1182-7. Am J Hum Genet. 1994. PMID: 7977378 Free PMC article.

5

Positional cloning of the gene associated with X-linked juvenile retinoschisis.

Sauer CG, Gehrig A, Warneke-Wittstock R, Marquardt A, Ewing CC, Gibson A, Lorenz B, Jurklies B, Weber BH. Sauer CG, et al. Among authors: weber bh. Nat Genet. 1997 Oct;17(2):164-70. doi: 10.1038/ng1097-164. Nat Genet. 1997. PMID: 9326935

6

The natural history of X-linked retinoschisis.

Roesch MT, Ewing CC, Gibson AE, Weber BH. Roesch MT, et al. Among authors: weber bh. Can J Ophthalmol. 1998 Apr;33(3):149-58. Can J Ophthalmol. 1998. PMID: 9606571

7

Autosomal recessive Sorsby fundus dystrophy revisited: molecular evidence for dominant inheritance.

Felbor U, Suvanto EA, Forsius HR, Eriksson AW, Weber BH. Felbor U, et al. Among authors: weber bh. Am J Hum Genet. 1997 Jan;60(1):57-62. Am J Hum Genet. 1997. PMID: 8981947 Free PMC article.

8

A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy.

Felbor U, Stöhr H, Amann T, Schönherr U, Apfelstedt-Sylla E, Weber BH. Felbor U, et al. Among authors: weber bh. J Med Genet. 1996 Mar;33(3):233-6. doi: 10.1136/jmg.33.3.233. J Med Genet. 1996. PMID: 8728699 Free PMC article.

9

An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1).

Sauer CG, Schworm HD, Ulbig M, Blankenagel A, Rohrschneider K, Pauleikhoff D, Grimm T, Weber BH. Sauer CG, et al. Among authors: weber bh. J Med Genet. 1997 Dec;34(12):961-6. doi: 10.1136/jmg.34.12.961. J Med Genet. 1997. PMID: 9429134 Free PMC article.

10

[Sorsby's fundus dystrophy. A genetically homogeneous disease].

Felbor U, Weber BH. Felbor U, et al. Among authors: weber bh. Ophthalmologe. 1998 May;95(5):287-90. doi: 10.1007/s003470050274. Ophthalmologe. 1998. PMID: 9643018 German.

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