Liehr T - Search Results

1

A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding.

Heller A, Starke H, Trifonov V, Rubtsov N, Wedding U, Loncarevic I, Bleck C, Claussen U, Liehr T. Heller A, et al. Among authors: liehr t. Int J Oncol. 2002 Jun;20(6):1179-81. Int J Oncol. 2002. PMID: 12011996

2

Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13.

Gebhart E, Liehr T, Wolff E, Ries J, Fiedler W, Steininger H, Koscielny S, Girod S. Gebhart E, et al. Among authors: liehr t. Int J Oncol. 1998 May;12(5):1151-5. doi: 10.3892/ijo.12.5.1151. Int J Oncol. 1998. PMID: 9538142

3

Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.

Liehr T, Starke H, Beensen V, Kähler C, Harbich M, Brude E, Ziegler M, Claussen U. Liehr T, et al. Int J Mol Med. 1999 Jan;3(1):11-4. doi: 10.3892/ijmm.3.1.11. Int J Mol Med. 1999. PMID: 9864379

4

Deletion monitoring in skin tumors by interphase-FISH using band-specific DNA probes.

Dobler M, Schuh J, Kiesewetter F, Schell H, Liehr T, Gebhart E. Dobler M, et al. Among authors: liehr t. Int J Oncol. 1999 Mar;14(3):571-6. doi: 10.3892/ijo.14.3.571. Int J Oncol. 1999. PMID: 10024693

5

Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3.

Liehr T, Kuhlenbäumer G, Wulf P, Taylor V, Suter U, Van Broeckhoven C, Lupski JR, Claussen U, Rautenstrauss B. Liehr T, et al. Genomics. 1999 May 15;58(1):106-8. doi: 10.1006/geno.1999.5803. Genomics. 1999. PMID: 10331954 No abstract available.

6

Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.

Starke H, Schreyer I, Kähler C, Fiedler W, Beensen V, Heller A, Nietzel A, Claussen U, Liehr T. Starke H, et al. Among authors: liehr t. Prenat Diagn. 1999 Dec;19(12):1169-74. Prenat Diagn. 1999. PMID: 10590438 Review.

7

Patterns of genomic imbalances in human solid tumors (Review).

Gebhart E, Liehr T. Gebhart E, et al. Among authors: liehr t. Int J Oncol. 2000 Feb;16(2):383-99. doi: 10.3892/ijo.16.2.383. Int J Oncol. 2000. PMID: 10639584 Review.

8

Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.

Heller A, Chudoba I, Bleck C, Senger G, Claussen U, Liehr T. Heller A, et al. Among authors: liehr t. Int J Oncol. 2000 Mar;16(3):461-8. Int J Oncol. 2000. PMID: 10675476

9

Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12th week of life.

Hübler A, Seidel J, Kauf E, Schramm D, Beensen V, Heller A, Liehr T, Zintl F. Hübler A, et al. Among authors: liehr t. J Pediatr Endocrinol Metab. 2000 Apr;13(4):445-50. doi: 10.1515/jpem.2000.13.4.445. J Pediatr Endocrinol Metab. 2000. PMID: 10777002

10

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.

Heller A, Seidel J, Hübler A, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T. Heller A, et al. Among authors: liehr t. J Med Genet. 2000 Jul;37(7):529-32. doi: 10.1136/jmg.37.7.529. J Med Genet. 2000. PMID: 10882757 Free PMC article.

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