Claussen U - Search Results

1

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: claussen u. Prenat Diagn. 2001 Dec;21(12):1049-52. doi: 10.1002/pd.192. Prenat Diagn. 2001. PMID: 11746162

2

Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding.

Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Claussen U, Liehr T. Mrasek K, et al. Among authors: claussen u. Int J Mol Med. 2003 Aug;12(2):139-46. Int J Mol Med. 2003. PMID: 12851708

3

Microdissection-derived murine mcb probes from somatic cell hybrids.

Trifonov V, Karst C, Claussen U, Mrasek K, Michel S, Avner P, Liehr T. Trifonov V, et al. Among authors: claussen u. J Histochem Cytochem. 2005 Jun;53(6):791-2. doi: 10.1369/jhc.4B6598.2005. J Histochem Cytochem. 2005. PMID: 15928329

4

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. Among authors: claussen u. Int J Mol Med. 2002 Apr;9(4):335-9. Int J Mol Med. 2002. PMID: 11891523

5

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. Among authors: claussen u. Fetal Diagn Ther. 2002 May-Jun;17(3):133-6. doi: 10.1159/000048025. Fetal Diagn Ther. 2002. PMID: 11914563

6

Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.

Senger G, Chudoba I, Friedrich U, Tommerup N, Claussen U, Brøndum-Nielsen K. Senger G, et al. Among authors: claussen u. Prenat Diagn. 1997 Apr;17(4):369-74. Prenat Diagn. 1997. PMID: 9160390

7

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: claussen u. Prenat Diagn. 1999 Dec;19(12):1169-74. Prenat Diagn. 1999. PMID: 10590438 Review.

8

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: claussen u. 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.

9

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: claussen u. Cytogenet Cell Genet. 2001;93(3-4):242-8. doi: 10.1159/000056991. Cytogenet Cell Genet. 2001. PMID: 11528119

10

Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.

Liehr T, Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Weier HU, Claussen U. Liehr T, et al. Among authors: claussen u. Cytogenet Genome Res. 2002;97(1-2):43-50. doi: 10.1159/000064043. Cytogenet Genome Res. 2002. PMID: 12438737

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