Weise A - Search Results

1

Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.

Carreira IM, Melo JB, Rodrigues C, Backx L, Vermeesch J, Weise A, Kosyakova N, Oliveira G, Matoso E. Carreira IM, et al. Among authors: weise a. Mol Cytogenet. 2009 Aug 4;2:16. doi: 10.1186/1755-8166-2-16. Mol Cytogenet. 2009. PMID: 19653912 Free PMC article.

2

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR. Liehr T, et al. Among authors: weise a. Am J Med Genet A. 2006 Jan 1;140(1):46-51. doi: 10.1002/ajmg.a.31048. Am J Med Genet A. 2006. PMID: 16333826 Review.

3

Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines.

Brecevic L, Michel S, Starke H, Müller K, Kosyakova N, Mrasek K, Weise A, Liehr T. Brecevic L, et al. Among authors: weise a. Cytogenet Genome Res. 2006;114(3-4):319-24. doi: 10.1159/000094220. Cytogenet Genome Res. 2006. PMID: 16954673

4

Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.

Pietrzak J, Mrasek K, Obersztyn E, Stankiewicz P, Kosyakova N, Weise A, Cheung SW, Cai WW, von Eggeling F, Mazurczak T, Bocian E, Liehr T. Pietrzak J, et al. Among authors: weise a. J Appl Genet. 2007;48(2):167-75. doi: 10.1007/BF03194675. J Appl Genet. 2007. PMID: 17495351

5

Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set.

Weise A, Mrasek K, Fickelscher I, Claussen U, Cheung SW, Cai WW, Liehr T, Kosyakova N. Weise A, et al. J Histochem Cytochem. 2008 May;56(5):487-93. doi: 10.1369/jhc.2008.950550. Epub 2008 Feb 5. J Histochem Cytochem. 2008. PMID: 18256020 Free PMC article.

6

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

Trifonov V, Fluri S, Binkert F, Nandini A, Anderson J, Rodriguez L, Gross M, Kosyakova N, Mkrtchyan H, Ewers E, Reich D, Weise A, Liehr T. Trifonov V, et al. Among authors: weise a. Mol Cytogenet. 2008 Apr 15;1:6. doi: 10.1186/1755-8166-1-6. Mol Cytogenet. 2008. PMID: 18471318 Free PMC article.

7

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report.

Manolakos E, Kosyakova N, Thomaidis L, Neroutsou R, Weise A, Mihalatos M, Orru S, Kokotas H, Kitsos G, Liehr T, Petersen MB. Manolakos E, et al. Among authors: weise a. Mol Cytogenet. 2008 Nov 11;1:24. doi: 10.1186/1755-8166-1-24. Mol Cytogenet. 2008. PMID: 19014423 Free PMC article.

8

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.

Kitsiou-Tzeli S, Manolakos E, Lagou M, Kontodiou M, Kosyakova N, Ewers E, Weise A, Garas A, Orru S, Liehr T, Metaxotou A. Kitsiou-Tzeli S, et al. Among authors: weise a. Mol Cytogenet. 2009 Jan 7;2:1. doi: 10.1186/1755-8166-2-1. Mol Cytogenet. 2009. PMID: 19128450 Free PMC article.

9

The hierarchically organized splitting of chromosomal bands for all human chromosomes.

Kosyakova N, Weise A, Mrasek K, Claussen U, Liehr T, Nelle H. Kosyakova N, et al. Among authors: weise a. Mol Cytogenet. 2009 Jan 26;2:4. doi: 10.1186/1755-8166-2-4. Mol Cytogenet. 2009. PMID: 19171032 Free PMC article.

10

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.

Kitsiou-Tzeli S, Manolakos E, Lagou M, Anagnostopoulou K, Kontodiou M, Kosyakova N, Ewers E, Weise A, Garas A, Orru S, Liehr T, Metaxotou A. Kitsiou-Tzeli S, et al. Among authors: weise a. Mol Cytogenet. 2009 Feb 20;2:8. doi: 10.1186/1755-8166-2-8. Mol Cytogenet. 2009. PMID: 19232114 Free PMC article. No abstract available.

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