Fischer C - Search Results

1

Non-random radial higher-order chromatin arrangements in nuclei of diploid human cells.

Cremer M, von Hase J, Volm T, Brero A, Kreth G, Walter J, Fischer C, Solovei I, Cremer C, Cremer T. Cremer M, et al. Among authors: fischer c. Chromosome Res. 2001;9(7):541-67. doi: 10.1023/a:1012495201697. Chromosome Res. 2001. PMID: 11721953

2

Evaluation of the utility of interphase cytogenetics to detect residual cells with a malignant genotype in mixed cell populations: a Burkitt lymphoma model.

Ried T, Lengauer C, Lipp M, Fischer C, Cremer T, Ward DC. Ried T, et al. Among authors: fischer c. DNA Cell Biol. 1993 Sep;12(7):637-43. doi: 10.1089/dna.1993.12.637. DNA Cell Biol. 1993. PMID: 8397822 Free article.

3

Chromosome aberration analysis in atomic bomb survivors and Thorotrast patients using two- and three-colour chromosome painting of chromosomal subsets.

Tanaka K, Popp S, Fischer C, Van Kaick G, Kamada N, Cremer T, Cremer C. Tanaka K, et al. Among authors: fischer c. Int J Radiat Biol. 1996 Jul;70(1):95-108. doi: 10.1080/095530096145373. Int J Radiat Biol. 1996. PMID: 8691041

4

High-resolution comparative hybridization to combed DNA fibers.

Kraus J, Weber RG, Cremer M, Seebacher T, Fischer C, Schurra C, Jauch A, Lichter P, Bensimon A, Cremer T. Kraus J, et al. Among authors: fischer c. Hum Genet. 1997 Mar;99(3):374-80. doi: 10.1007/s004390050375. Hum Genet. 1997. PMID: 9050926

5

Modelling germline mosaicism and different new mutation rates simultaneously for appropriate risk calculations in families with Duchenne muscular dystrophy.

Fischer C, Gross W, Krüger J, Cremer M, Vogel F, Grimm T. Fischer C, et al. Ann Hum Genet. 2006 Mar;70(Pt 2):237-48. doi: 10.1111/j.1469-1809.2005.00226.x. Ann Hum Genet. 2006. PMID: 16626333

6

Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis.

Scholz I, Popp S, Granzow M, Schoell B, Holtgreve-Grez H, Takeuchi S, Schrappe M, Harbott J, Teigler-Schlegel A, Zimmermann M, Fischer C, Koeffler HP, Bartram CR, Jauch A. Scholz I, et al. Among authors: fischer c. Cancer Genet Cytogenet. 2001 Jan 15;124(2):89-97. doi: 10.1016/s0165-4608(00)00330-7. Cancer Genet Cytogenet. 2001. PMID: 11172898

7

Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?

Evers C, Heidemann PH, Dunstheimer D, Schulze E, Haag C, Janssen JW, Fischer C, Jauch A, Moog U. Evers C, et al. Among authors: fischer c. Clin Genet. 2011 May;79(5):489-94. doi: 10.1111/j.1399-0004.2010.01488.x. Clin Genet. 2011. PMID: 20681991

8

Elevated DNA sequence diversity in the genomic region of the phosphatase PPP2R3L gene in the human pseudoautosomal region.

Schiebel K, Meder J, Rump A, Rosenthal A, Winkelmann M, Fischer C, Bonk T, Humeny A, Rappold G. Schiebel K, et al. Among authors: fischer c. Cytogenet Cell Genet. 2000;91(1-4):224-30. doi: 10.1159/000056849. Cytogenet Cell Genet. 2000. PMID: 11173861

9

Chromosomal aberrations in sporadic pituitary tumors.

Trautmann K, Thakker RV, Ellison DW, Ibrahim A, Lees PD, Harding B, Fischer C, Popp S, Bartram CR, Jauch A. Trautmann K, et al. Among authors: fischer c. Int J Cancer. 2001 Mar 15;91(6):809-14. doi: 10.1002/1097-0215(200102)9999:9999<::aid-ijc1127>3.0.co;2-e. Int J Cancer. 2001. PMID: 11275984 Free article.

10

D20S19, linked to low voltage EEG, benign neonatal convulsions, and Fanconi anaemia, maps to a region of enhanced recombination and is localized between CpG islands.

Steinlein O, Fischer C, Keil R, Smigrodzki R, Vogel F. Steinlein O, et al. Among authors: fischer c. Hum Mol Genet. 1992 Aug;1(5):325-9. doi: 10.1093/hmg/1.5.325. Hum Mol Genet. 1992. PMID: 1303209

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