Ziegler M - 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: ziegler m. 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

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.

3

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: ziegler m. Prenat Diagn. 2001 May;21(5):419-21. doi: 10.1002/pd.44. Prenat Diagn. 2001. PMID: 11360288 No abstract available.

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

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

6

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

7

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

8

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

9

X-autosome and X-Y Translocations in Female Carriers: X-chromosome Inactivation Easily Detectable by 5-ethynyl-2-deoxyuridine (EdU).

Donat M, Louis A, Kreskowski K, Ziegler M, Weise A, Schreyer I, Liehr T. Donat M, et al. Among authors: ziegler m. Balkan J Med Genet. 2017 Jun 30;20(1):87-90. doi: 10.1515/bjmg-2017-0012. eCollection 2017 Jun 30. Balkan J Med Genet. 2017. PMID: 28924545 Free PMC article.

10

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

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