Liehr T - Search Results

1

New Insights into Phasmatodea Chromosomes.

Liehr T, Buleu O, Karamysheva T, Bugrov A, Rubtsov N. Liehr T, et al. Genes (Basel). 2017 Nov 17;8(11):327. doi: 10.3390/genes8110327. Genes (Basel). 2017. PMID: 29149047 Free PMC article.

2

Zoo-FISH with region-specific paints for mink chromosome 5q: delineation of inter- and intrachromosomal rearrangements in human, pig, and fox.

Rubtsov NB, Karamisheva TV, Astakhova NM, Liehr T, Claussen U, Zhdanova NS. Rubtsov NB, et al. Among authors: liehr t. Cytogenet Cell Genet. 2000;90(3-4):268-70. doi: 10.1159/000056786. Cytogenet Cell Genet. 2000. PMID: 11124531

3

Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia.

Starke H, Raida M, Trifonov V, Clement JH, Loncarevic IF, Heller A, Bleck C, Nietzel A, Rubtsov N, Claussen U, Liehr T. Starke H, et al. Among authors: liehr t. Br J Haematol. 2001 May;113(2):435-8. doi: 10.1046/j.1365-2141.2001.02787.x. Br J Haematol. 2001. PMID: 11380412 Free article.

4

Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB).

Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Rocchi M, Claussen U, Liehr T. Mrasek K, et al. Among authors: liehr t. Cytogenet Cell Genet. 2001;93(3-4):242-8. doi: 10.1159/000056991. Cytogenet Cell Genet. 2001. PMID: 11528119

5

Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.

Dufke A, Walczak C, Liehr T, Starke H, Trifonov V, Rubtsov N, Schöning M, Enders H, Eggermann T. Dufke A, et al. Among authors: liehr t. Eur J Hum Genet. 2001 Aug;9(8):572-6. doi: 10.1038/sj.ejhg.5200673. Eur J Hum Genet. 2001. PMID: 11528501

6

Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).

Starke H, Senger G, Kossakiewicz M, Tittelbach H, Rau D, Rubtsov N, Trifonov V, Heller A, Hartmann I, Claussen U, Liehr T. Starke H, et al. Among authors: liehr t. Prenat Diagn. 2001 Dec;21(12):1049-52. doi: 10.1002/pd.192. Prenat Diagn. 2001. PMID: 11746162

7

Microdissection based high resolution multicolor banding for all 24 human chromosomes.

Liehr T, Heller A, Starke H, Rubtsov N, Trifonov V, Mrasek K, Weise A, Kuechler A, Claussen U. Liehr T, et al. Int J Mol Med. 2002 Apr;9(4):335-9. Int J Mol Med. 2002. PMID: 11891523

8

First case of trisomy 13 plus mosaic trisomy 1q.

Liehr T, Schmidt M, Starke H, Ziegler M, Kittner G, Heller A, Rubtsov N, Trifonov V, Claussen U. Liehr T, et al. Fetal Diagn Ther. 2002 May-Jun;17(3):133-6. doi: 10.1159/000048025. Fetal Diagn Ther. 2002. PMID: 11914563

9

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

10

The DNA-based structure of human chromosome 5 in interphase.

Lemke J, Claussen J, Michel S, Chudoba I, Mühlig P, Westermann M, Sperling K, Rubtsov N, Grummt UW, Ullmann P, Kromeyer-Hauschild K, Liehr T, Claussen U. Lemke J, et al. Among authors: liehr t. Am J Hum Genet. 2002 Nov;71(5):1051-9. doi: 10.1086/344286. Epub 2002 Oct 7. Am J Hum Genet. 2002. PMID: 12370837 Free PMC article.

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