Weise A - Search Results

1

Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Melo JB, Backx L, Vermeesch JR, Santos HG, Sousa AC, Kosyakova N, Weise A, von Eggeling F, Liehr T, Carreira IM. Melo JB, et al. Among authors: weise a. J Appl Genet. 2011 May;52(2):193-200. doi: 10.1007/s13353-011-0035-3. Epub 2011 Mar 25. J Appl Genet. 2011. PMID: 21437654 Review.

2

Microdissection based high resolution multicolor banding for all 24 human chromosomes.

Liehr T, Heller A, Starke H, Rubtsov N, Trifonov V, Mrasek K, Weise A, Kuechler A, Claussen U. Liehr T, et al. Among authors: weise a. Int J Mol Med. 2002 Apr;9(4):335-9. Int J Mol Med. 2002. PMID: 11891523

3

Evidence for interphase DNA decondensation transverse to the chromosome axis: a multicolor banding analysis.

Weise A, Starke H, Heller A, Uwe C, Liehr T. Weise A, et al. Int J Mol Med. 2002 Apr;9(4):359-61. Int J Mol Med. 2002. PMID: 11891527

4

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.

Weise A, Starke H, Heller A, Tönnies H, Volleth M, Stumm M, Gabriele S, Nietzel A, Claussen U, Liehr T. Weise A, et al. J Med Genet. 2002 Jun;39(6):434-9. doi: 10.1136/jmg.39.6.434. J Med Genet. 2002. PMID: 12070255 Free PMC article. No abstract available.

5

Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.

Liehr T, Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Weier HU, Claussen U. Liehr T, et al. Among authors: weise a. Cytogenet Genome Res. 2002;97(1-2):43-50. doi: 10.1159/000064043. Cytogenet Genome Res. 2002. PMID: 12438737

6

Fluorescence in situ hybridization (FISH) on human chromosomes using photoprobe biotin-labeled probes.

Weise A, Harbarth P, Claussen U, Liehr T. Weise A, et al. J Histochem Cytochem. 2003 Apr;51(4):549-51. doi: 10.1177/002215540305100418. J Histochem Cytochem. 2003. PMID: 12642635

7

Evidence for a new microdeletion syndrome in 15q21.

Liehr T, Starke H, Heller A, Weise A, Beensen V, Senger G, Kittner G, Prechtel M, Claussen U, Seidel J. Liehr T, et al. Among authors: weise a. Int J Mol Med. 2003 May;11(5):575-7. doi: 10.3892/ijmm.11.5.575. Int J Mol Med. 2003. PMID: 12684692

8

Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines.

Weise A, Liehr T, Efferth T, Kuechler A, Gebhart E. Weise A, et al. Cytogenet Genome Res. 2002;98(2-3):118-25. doi: 10.1159/000069808. Cytogenet Genome Res. 2002. PMID: 12697993

9

Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis.

von Eggeling F, Langer S, Hoppe C, Liehr T, Weise A, Lederer G, Kotzot D. von Eggeling F, et al. Among authors: weise a. Clin Genet. 2003 Aug;64(2):168-71. doi: 10.1034/j.1399-0004.2003.00102.x. Clin Genet. 2003. PMID: 12859416 No abstract available.

10

Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10].

Sauter S, von Beust G, Burfeind P, Weise A, Starke H, Liehr T, Zoll B. Sauter S, et al. Among authors: weise a. Am J Med Genet A. 2003 Aug 1;120A(4):533-6. doi: 10.1002/ajmg.a.20089. Am J Med Genet A. 2003. PMID: 12884434

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