Ziegler M - Search Results

1

De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features.

Varvagiannis K, Papoulidis I, Koromila T, Kefalas K, Ziegler M, Liehr T, Petersen MB, Gyftodimou Y, Manolakos E. Varvagiannis K, et al. Among authors: ziegler m. Meta Gene. 2014 Apr 15;2:274-82. doi: 10.1016/j.mgene.2014.03.004. eCollection 2014 Dec. Meta Gene. 2014. PMID: 25606410 Free PMC article.

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

3

Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia.

Loncarevic IF, Römer J, Starke H, Heller A, Bleck C, Ziegler M, Fiedler W, Liehr T, Clement JH, Claussen U. Loncarevic IF, et al. Among authors: ziegler m. Genes Chromosomes Cancer. 2002 Jun;34(2):193-200. doi: 10.1002/gcc.10056. Genes Chromosomes Cancer. 2002. PMID: 11979553

4

Rapid prenatal diagnostics in the interphase nucleus: procedure and cut-off rates.

Liehr T, Ziegler M. Liehr T, et al. Among authors: ziegler m. J Histochem Cytochem. 2005 Mar;53(3):289-91. doi: 10.1369/jhc.4B6394.2005. J Histochem Cytochem. 2005. PMID: 15750004

5

A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection.

Kuechler A, Ziegler M, Blank C, Rommel B, Bullerdiek J, Ahrens J, Claussen U, Liehr T. Kuechler A, et al. Among authors: ziegler m. J Histochem Cytochem. 2005 Mar;53(3):355-7. doi: 10.1369/jhc.4B6437.2005. J Histochem Cytochem. 2005. PMID: 15750018

6

A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report.

Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Desai M, Andrieux J, Vermeesch J, Hamid AB, Ziegler M, Liehr T. Sheth F, et al. Among authors: ziegler m. Mol Cytogenet. 2009 Nov 12;2:22. doi: 10.1186/1755-8166-2-22. Mol Cytogenet. 2009. PMID: 19909521 Free PMC article.

7

Small supernumerary marker chromosomes 1 with a normal phenotype.

Liehr T, Wegner RD, Stumm M, Martin T, Gillessen-Kaesbach G, Kosyakova N, Ewers E, Hamid AB, von Eggeling F, Hentschel J, Ziegler M, Weise A. Liehr T, et al. Among authors: ziegler m. J Chin Med Assoc. 2010 Apr;73(4):205-7. doi: 10.1016/S1726-4901(10)70042-3. J Chin Med Assoc. 2010. PMID: 20457442 Free article.

8

Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: molecular cytogenetic analysis and review of the literature.

Manolakos E, Peitsidis P, Eleftheriades M, Dedoulis E, Ziegler M, Orru S, Liehr T, Petersen MB. Manolakos E, et al. Among authors: ziegler m. J Obstet Gynaecol Res. 2010 Apr;36(2):435-40. doi: 10.1111/j.1447-0756.2009.01140.x. J Obstet Gynaecol Res. 2010. PMID: 20492403

9

Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report.

Fernández-Toral J, Rodríguez L, Plasencia A, Martínez-Frías ML, Ewers E, Hamid AB, Ziegler M, Liehr T. Fernández-Toral J, et al. Among authors: ziegler m. J Med Case Rep. 2010 Aug 3;4:239. doi: 10.1186/1752-1947-4-239. J Med Case Rep. 2010. PMID: 20682055 Free PMC article.

10

New cytogenetically visible copy number variant in region 8q21.2.

Manvelyan M, Cremer FW, Lancé J, Kläs R, Kelbova C, Ramel C, Reichenbach H, Schmidt C, Ewers E, Kreskowski K, Ziegler M, Kosyakova N, Liehr T. Manvelyan M, et al. Among authors: ziegler m. Mol Cytogenet. 2011 Jan 5;4(1):1. doi: 10.1186/1755-8166-4-1. Mol Cytogenet. 2011. PMID: 21208402 Free PMC article.

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