Brandt B - Search Results

1

Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma.

Szijan I, Lohmann DR, Parma DL, Brandt B, Horsthemke B. Szijan I, et al. Among authors: brandt b. J Med Genet. 1995 Jun;32(6):475-9. doi: 10.1136/jmg.32.6.475. J Med Genet. 1995. PMID: 7666401 Free PMC article.

2

Spectrum of small length germline mutations in the RB1 gene.

Lohmann DR, Brandt B, Höpping W, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: brandt b. Hum Mol Genet. 1994 Dec;3(12):2187-93. doi: 10.1093/hmg/3.12.2187. Hum Mol Genet. 1994. PMID: 7881418

3

Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma.

Lohmann DR, Brandt B, Höpping W, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: brandt b. Hum Genet. 1994 Oct;94(4):349-54. doi: 10.1007/BF00201591. Hum Genet. 1994. PMID: 7927327

4

The spectrum of RB1 germ-line mutations in hereditary retinoblastoma.

Lohmann DR, Brandt B, Höpping W, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: brandt b. Am J Hum Genet. 1996 May;58(5):940-9. Am J Hum Genet. 1996. PMID: 8651278 Free PMC article.

5

Molecular analysis and predictive testing in retinoblastoma.

Lohmann DR, Brandt B, Oehlschläger U, Göttmann E, Höpping W, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: brandt b. Ophthalmic Genet. 1995 Dec;16(4):135-42. doi: 10.3109/13816819509057854. Ophthalmic Genet. 1995. PMID: 8749049

6

[Molecular genetics and diagnosis of retinoblastoma. Significance for ophthalmologic practice].

Lohmann DR, Brandt B, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: brandt b. Ophthalmologe. 1997 Apr;94(4):263-7. doi: 10.1007/s003470050110. Ophthalmologe. 1997. PMID: 9229493 Review. German.

7

Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.

Lohmann DR, Gerick M, Brandt B, Oelschläger U, Lorenz B, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: brandt b. Am J Hum Genet. 1997 Aug;61(2):282-94. doi: 10.1086/514845. Am J Hum Genet. 1997. PMID: 9311732 Free PMC article.

8

Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastoma.

Horsthemke B, Brandt B, Albrecht B, Passarge E. Horsthemke B, et al. Among authors: brandt b. Am J Med Genet. 1992 Sep 15;44(2):255. doi: 10.1002/ajmg.1320440235. Am J Med Genet. 1992. PMID: 1456305 No abstract available.

9

Methylation analysis of several tumour suppressor genes shows a low frequency of methylation of CDKN2A and RARB in uveal melanomas.

Zeschnigk M, Tschentscher F, Lich C, Brandt B, Horsthemke B, Lohmann DR. Zeschnigk M, et al. Among authors: brandt b. Comp Funct Genomics. 2003;4(3):329-36. doi: 10.1002/cfg.295. Comp Funct Genomics. 2003. PMID: 18629284 Free PMC article.

10

A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma gene.

Brandt B, Greger V, Yandell D, Passarge E, Horsthemke B. Brandt B, et al. Am J Hum Genet. 1992 Dec;51(6):1450-1. Am J Hum Genet. 1992. PMID: 1463022 Free PMC article. No abstract available.

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