Claussen U - Search Results

1

First postnatal case of mosaic del(22)/r(22).

Starke H, Mitulla B, Beensen V, Trifonov V, Rubtsov N, Heller A, Ziegler M, Neumann A, Claussen U, Liehr T. Starke H, et al. Among authors: claussen u. Prenat Diagn. 2003 Sep;23(9):765-7. doi: 10.1002/pd.666. Prenat Diagn. 2003. PMID: 12975792 No abstract available.

2

Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei.

Liehr T, Schreyer I, Neumann A, Beensen V, Ziegler M, Hartmann I, Starke H, Heller A, Nietzel A, Claussen U. Liehr T, et al. Among authors: claussen u. Prenat Diagn. 2002 Jun;22(6):497-9. doi: 10.1002/pd.299. Prenat Diagn. 2002. PMID: 12116314 No abstract available.

3

Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter.

Trifonov V, Seidel J, Starke H, Martina P, Beensen V, Ziegler M, Hartmann I, Heller A, Nietzel A, Claussen U, Liehr T. Trifonov V, et al. Among authors: claussen u. Prenat Diagn. 2003 May;23(5):427-30. doi: 10.1002/pd.595. Prenat Diagn. 2003. PMID: 12749042 No abstract available.

4

Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).

Liehr T, Heller A, Eichhorn KH, Beensen V, Schulze E, Starke H, Claussen U, Schreyer I. Liehr T, et al. Among authors: claussen u. Prenat Diagn. 2004 Dec 15;24(12):1022-4. doi: 10.1002/pd.971. Prenat Diagn. 2004. PMID: 15614895 No abstract available.

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

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.

7

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

8

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: claussen u. Int J Oncol. 2002 Jun;20(6):1179-81. Int J Oncol. 2002. PMID: 12011996

9

Pitfalls of rapid prenatal diagnosis using the interphase nucleus.

Liehr T, Beensen V, Hauschild R, Ziegler M, Hartmann I, Starke H, Heller A, Kähler C, Schmidt M, Reiber W, Hesse M, Claussen U. Liehr T, et al. Among authors: claussen u. Prenat Diagn. 2001 May;21(5):419-21. doi: 10.1002/pd.44. Prenat Diagn. 2001. PMID: 11360288 No abstract available.

10

Highly complex karyotypic changes in acute myelogenous leukemia: a case report.

Heller A, Rubtsov N, Kytölä S, Karamysheva TV, Sablina OV, Degtyareva MM, Starke H, Metzke H, Claussen U, Liehr T. Heller A, et al. Among authors: claussen u. Int J Oncol. 2003 Jul;23(1):139-43. Int J Oncol. 2003. PMID: 12792786

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