Starke H - Search Results

1

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

2

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: starke h. Fetal Diagn Ther. 2002 May-Jun;17(3):133-6. doi: 10.1159/000048025. Fetal Diagn Ther. 2002. PMID: 11914563

3

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.

4

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements.

Starke H, Seidel J, Henn W, Reichardt S, Volleth M, Stumm M, Behrend C, Sandig KR, Kelbova C, Senger G, Albrecht B, Hansmann I, Heller A, Claussen U, Liehr T. Starke H, et al. Eur J Hum Genet. 2002 Dec;10(12):790-800. doi: 10.1038/sj.ejhg.5200889. Eur J Hum Genet. 2002. PMID: 12461685

5

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

6

Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS.

Heller A, Trifonov V, Rubtsov N, Sauerbrey A, Starke H, Loncarevic IF, Claussen U, Liehr T. Heller A, et al. Among authors: starke h. Oncol Rep. 2003 Nov-Dec;10(6):1789-92. doi: 10.3892/or.10.6.1789. Oncol Rep. 2003. PMID: 14534697

7

Characterization of a highly aberrant plasma cell leukemia karyotype: a case report.

Heller A, Fricke HJ, Starke H, Loncarevic IF, Claussen U, Liehr T. Heller A, et al. Among authors: starke h. Oncol Rep. 2004 Jan;11(1):89-92. Oncol Rep. 2004. PMID: 14654908

8

Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.

Liehr T, Brude E, Gillessen-Kaesbach G, König R, Mrasek K, von Eggeling F, Starke H. Liehr T, et al. Among authors: starke h. Eur J Med Genet. 2005 Apr-Jun;48(2):175-81. doi: 10.1016/j.ejmg.2005.01.004. Epub 2005 Feb 17. Eur J Med Genet. 2005. PMID: 16053909 Review.

9

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR. Liehr T, et al. Among authors: starke h. Am J Med Genet A. 2006 Jan 1;140(1):46-51. doi: 10.1002/ajmg.a.31048. Am J Med Genet A. 2006. PMID: 16333826 Review.

10

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

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