Ziegler M - Search Results

1

Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement.

Manolakos E, Vetro A, Papadopoulou E, Kefalas K, Lagou M, Thomaidis L, Peitsidis P, Sifakis S, Divane A, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: ziegler m. Cytogenet Genome Res. 2013;140(1):12-20. doi: 10.1159/000350868. Epub 2013 May 4. Cytogenet Genome Res. 2013. PMID: 23652918

2

Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization.

Papadopoulou Z, Papoulidis I, Sifakis S, Markopoulos G, Vetro A, Vlaikou AM, Ziegler M, Liehr T, Thomaidis L, Zuffardi O, Syrrou M, George K, Manolakos E. Papadopoulou Z, et al. Among authors: ziegler m. Mol Med Rep. 2017 Dec;16(6):8808-8818. doi: 10.3892/mmr.2017.7760. Epub 2017 Oct 10. Mol Med Rep. 2017. PMID: 29039589 Free PMC article. Review.

3

A neocentric isochromosome Yp present as additional small supernumerary marker chromosome--evidence against U-type exchange mechanism?

Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Patil S, Ziegler M, Liehr T. Sheth F, et al. Among authors: ziegler m. Cytogenet Genome Res. 2009;125(2):115-6. doi: 10.1159/000227835. Epub 2009 Aug 31. Cytogenet Genome Res. 2009. PMID: 19729914

4

De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature.

Weise A, Rittinger O, Starke H, Ziegler M, Claussen U, Liehr T. Weise A, et al. Among authors: ziegler m. Cytogenet Genome Res. 2003;103(1-2):14-6. doi: 10.1159/000076284. Cytogenet Genome Res. 2003. PMID: 15004457

5

First case of a neocentromere formation in an otherwise normal chromosome 7.

Liehr T, Kosyakova N, Weise A, Ziegler M, Raabe-Meyer G. Liehr T, et al. Among authors: ziegler m. Cytogenet Genome Res. 2010 Jun;128(4):189-91. doi: 10.1159/000271471. Epub 2009 Dec 23. Cytogenet Genome Res. 2010. PMID: 20029167

6

Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.

Manolakos E, Kefalas K, Neroutsou R, Lagou M, Kosyakova N, Ewers E, Ziegler M, Weise A, Tsoplou P, Rapti SM, Papoulidis I, Anastasakis E, Garas A, Sotiriou S, Eleftheriades M, Peitsidis P, Malathrakis D, Thomaidis L, Kitsos G, Orru S, Liehr T, Petersen MB, Kitsiou-Tzeli S. Manolakos E, et al. Among authors: ziegler m. Mol Med Rep. 2010 Nov-Dec;3(6):1015-22. doi: 10.3892/mmr.2010.358. Epub 2010 Sep 10. Mol Med Rep. 2010. PMID: 21472348

7

Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown origin.

Klein E, Rocchi M, Ovens-Raeder A, Kosyakova N, Weise A, Ziegler M, Meins M, Morlot S, Fischer W, Volleth M, Polityko A, Ogilvie CM, Kraus C, Liehr T. Klein E, et al. Among authors: ziegler m. Cytogenet Genome Res. 2012;136(3):163-6. doi: 10.1159/000336648. Epub 2012 Mar 1. Cytogenet Genome Res. 2012. PMID: 22377933

8

Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements.

Liehr T, Kosayakova N, Schröder J, Ziegler M, Kreskowski K, Pohle B, Bhatt S, Theuss L, Wilhelm K, Weise A, Mrasek K. Liehr T, et al. Among authors: ziegler m. Balkan J Med Genet. 2011 Dec;14(2):13-6. doi: 10.2478/v10034-011-0042-z. Balkan J Med Genet. 2011. PMID: 24052707 Free PMC article.

9

Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.

Liehr T, Starke H, Beensen V, Kähler C, Harbich M, Brude E, Ziegler M, Claussen U. Liehr T, et al. Among authors: ziegler m. Int J Mol Med. 1999 Jan;3(1):11-4. doi: 10.3892/ijmm.3.1.11. Int J Mol Med. 1999. PMID: 9864379

10

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: ziegler m. 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.

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