Starke H - Search Results

1

Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism.

Liehr T, Ziegler M, Starke H, Heller A, Kuechler A, Kittner G, Beensen V, Seidel J, Hässler H, Müsebeck J, Claussen U. Liehr T, et al. Among authors: starke h. Clin Genet. 2003 Aug;64(2):166-7. doi: 10.1034/j.1399-0004.2003.00114.x. Clin Genet. 2003. PMID: 12859415 No abstract available.

2

FISH banding methods: applications in research and diagnostics.

Liehr T, Heller A, Starke H, Claussen U. Liehr T, et al. Among authors: starke h. Expert Rev Mol Diagn. 2002 May;2(3):217-25. doi: 10.1586/14737159.2.3.217. Expert Rev Mol Diagn. 2002. PMID: 12050860 Review.

3

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: starke h. 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.

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: starke h. Hum Genet. 2001 Mar;108(3):199-204. doi: 10.1007/s004390100459. Hum Genet. 2001. PMID: 11354630

5

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. Among authors: starke h. 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.

6

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: starke h. 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.

7

First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16.

Starke H, Mitulla B, Nietzel A, Heller A, Beensen V, Grosswendt G, Claussen U, von Eggeling F, Liehr T. Starke H, et al. Am J Med Genet A. 2003 Jan 1;116A(1):26-30. doi: 10.1002/ajmg.a.10830. Am J Med Genet A. 2003. PMID: 12476447

8

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.

Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M, Wegner RD, Seidel J, Schmidt A, Kuechler A, Schreyer I, Claussen U, von Eggeling F, Liehr T. Starke H, et al. Hum Genet. 2003 Dec;114(1):51-67. doi: 10.1007/s00439-003-1016-3. Epub 2003 Sep 16. Hum Genet. 2003. PMID: 13680362

9

FISH banding in tumor cytogenetics.

Liehr T, Gross M, Karst C, Glaser M, Mrasek K, Starke H, Weise A, Mkrtchyan H, Kuechler A. Liehr T, et al. Among authors: starke h. Cancer Genet Cytogenet. 2006 Jan 1;164(1):88-9. doi: 10.1016/j.cancergencyto.2005.06.013. Cancer Genet Cytogenet. 2006. PMID: 16364770 No abstract available.

10

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

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