Horsthemke 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: horsthemke 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

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 Free article.

3

Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 families.

Strumberg D, Hauffa BP, Horsthemke B, Grosse-Wilde H. Strumberg D, et al. Among authors: horsthemke b. Eur J Pediatr. 1992 Nov;151(11):821-6. doi: 10.1007/BF01957933. Eur J Pediatr. 1992. PMID: 1361434

4

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.

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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