Horsthemke B - Search Results

1

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

2

PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.

Horsthemke B, Claussen U, Hesse S, Lüdecke HJ. Horsthemke B, et al. PCR Methods Appl. 1992 May;1(4):229-33. doi: 10.1101/gr.1.4.229. PCR Methods Appl. 1992. PMID: 1282430

3

A new restriction fragment length polymorphism of the human TNF-B gene detected by AspHI digest.

Ferencik S, Lindemann M, Horsthemke B, Grosse-Wilde H. Ferencik S, et al. Among authors: horsthemke b. Eur J Immunogenet. 1992 Dec;19(6):425-30. doi: 10.1111/j.1744-313x.1992.tb00086.x. Eur J Immunogenet. 1992. PMID: 1362079 No abstract available.

4

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.

Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, Ledbetter SA, Greenberg F, Chinault AC, et al. Kuwano A, et al. Among authors: horsthemke b. Hum Mol Genet. 1992 Sep;1(6):417-25. doi: 10.1093/hmg/1.6.417. Hum Mol Genet. 1992. PMID: 1363801

5

Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanoma.

Horsthemke B, Prescher G, Bornfeld N, Becher R. Horsthemke B, et al. Genes Chromosomes Cancer. 1992 Apr;4(3):217-21. doi: 10.1002/gcc.2870040305. Genes Chromosomes Cancer. 1992. PMID: 1382562

6

Genetics and cytogenetics of retinoblastoma.

Horsthemke B. Horsthemke B. Cancer Genet Cytogenet. 1992 Oct 1;63(1):1-7. doi: 10.1016/0165-4608(92)90055-d. Cancer Genet Cytogenet. 1992. PMID: 1423220 Review.

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. 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

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

9

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.

Dittrich B, Robinson WP, Knoblauch H, Buiting K, Schmidt K, Gillessen-Kaesbach G, Horsthemke B. Dittrich B, et al. Among authors: horsthemke b. Hum Genet. 1992 Nov;90(3):313-5. doi: 10.1007/BF00220089. Hum Genet. 1992. PMID: 1487250

10

Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis.

Lohmann D, Horsthemke B, Gillessen-Kaesbach G, Stefani FH, Höfler H. Lohmann D, et al. Among authors: horsthemke b. Hum Genet. 1992 Apr;89(1):49-53. doi: 10.1007/BF00207041. Hum Genet. 1992. PMID: 1577465

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