Passarge E - Search Results

1

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. Among authors: passarge e. Am J Hum Genet. 1992 Dec;51(6):1450-1. Am J Hum Genet. 1992. PMID: 1463022 Free PMC article. No abstract available.

2

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: passarge e. Am J Hum Genet. 1996 May;58(5):940-9. Am J Hum Genet. 1996. PMID: 8651278 Free PMC article.

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: passarge e. Hum Genet. 1994 Oct;94(4):349-54. doi: 10.1007/BF00201591. Hum Genet. 1994. PMID: 7927327

4

Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma.

Greger V, Debus N, Lohmann D, Höpping W, Passarge E, Horsthemke B. Greger V, et al. Among authors: passarge e. Hum Genet. 1994 Nov;94(5):491-6. doi: 10.1007/BF00211013. Hum Genet. 1994. PMID: 7959682

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: passarge e. Ophthalmic Genet. 1995 Dec;16(4):135-42. doi: 10.3109/13816819509057854. Ophthalmic Genet. 1995. PMID: 8749049

6

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: passarge e. Am J Hum Genet. 1997 Aug;61(2):282-94. doi: 10.1086/514845. Am J Hum Genet. 1997. PMID: 9311732 Free PMC article.

7

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: passarge e. 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.

8

Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families.

Goddard AD, Phillips RA, Greger V, Passarge E, Höpping W, Zhu XP, Gallie BL, Horsthemke B. Goddard AD, et al. Among authors: passarge e. Clin Genet. 1990 Feb;37(2):117-26. doi: 10.1111/j.1399-0004.1990.tb03488.x. Clin Genet. 1990. PMID: 1968790

9

Somatic mosaicism in a patient with bilateral retinoblastoma.

Greger V, Passarge E, Horsthemke B. Greger V, et al. Among authors: passarge e. Am J Hum Genet. 1990 Jun;46(6):1187-93. Am J Hum Genet. 1990. PMID: 1971154 Free PMC article.

10

Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.

Kloss K, Währisch P, Greger V, Messmer E, Fritze H, Höpping W, Passarge E, Horsthemke B. Kloss K, et al. Among authors: passarge e. Am J Med Genet. 1991 May 1;39(2):196-200. doi: 10.1002/ajmg.1320390215. Am J Med Genet. 1991. PMID: 2063924

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