Liehr T - Search Results

1

Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?

Liehr T, Bartels I, Zoll B, Ewers E, Mrasek K, Kosyakova N, Merkas M, Hamid AB, von Eggeling F, Posorski N, Weise A. Liehr T, et al. Cytogenet Genome Res. 2011;132(1-2):121-3. doi: 10.1159/000316393. Epub 2010 Jul 20. Cytogenet Genome Res. 2011. PMID: 20639618

2

Localization of mariner DNA transposons in the human genome by PRINS.

Reiter LT, Liehr T, Rautenstrauss B, Robertson HM, Lupski JR. Reiter LT, et al. Among authors: liehr t. Genome Res. 1999 Sep;9(9):839-43. doi: 10.1101/gr.9.9.839. Genome Res. 1999. PMID: 10508842 Free PMC article.

3

A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients.

Bleichert A, Fiedler W, Claussen U, Ernst G, Loncarevic IF, Heller A, Liehr T, Kunert C, von Eggeling F. Bleichert A, et al. Among authors: liehr t. Int J Mol Med. 2001 Jun;7(6):591-5. doi: 10.3892/ijmm.7.6.591. Int J Mol Med. 2001. PMID: 11351270

4

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).

Nietzel A, Rocchi M, Starke H, Heller A, Fiedler W, Wlodarska I, Loncarevic IF, Beensen V, Claussen U, Liehr T. Nietzel A, et al. Among authors: liehr t. Hum Genet. 2001 Mar;108(3):199-204. doi: 10.1007/s004390100459. Hum Genet. 2001. PMID: 11354630

5

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.

6

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

7

Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21.

Liehr T, Beensen V, Starke H, Hauschild R, Hempell E, Fritsche V, Hoppe C, Grosswendt G, Prechtel M, Ziegler M, Claussen U, von Eggeling F. Liehr T, et al. Clin Genet. 2001 Jul;60(1):83-5. doi: 10.1034/j.1399-0004.2001.600114.x. Clin Genet. 2001. PMID: 11531976 No abstract available.

8

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

9

Evidence for interphase DNA decondensation transverse to the chromosome axis: a multicolor banding analysis.

Weise A, Starke H, Heller A, Uwe C, Liehr T. Weise A, et al. Among authors: liehr t. Int J Mol Med. 2002 Apr;9(4):359-61. Int J Mol Med. 2002. PMID: 11891527

10

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.

Weise A, Starke H, Heller A, Tönnies H, Volleth M, Stumm M, Gabriele S, Nietzel A, Claussen U, Liehr T. Weise A, et al. Among authors: liehr t. J Med Genet. 2002 Jun;39(6):434-9. doi: 10.1136/jmg.39.6.434. J Med Genet. 2002. PMID: 12070255 Free PMC article. No abstract available.

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