Haaf T - Search Results

1

Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infections.

Yue Y, Stout K, Grossmann B, Zechner U, Brinckmann A, White C, Pilz DT, Haaf T. Yue Y, et al. Among authors: haaf t. J Med Genet. 2006 Feb;43(2):143-7. doi: 10.1136/jmg.2004.029660. Epub 2005 May 20. J Med Genet. 2006. PMID: 15908570 Free PMC article.

2

Complex chromosomal rearrangement in a woman with multiple miscarriages.

Kausch K, Haaf T, Köhler J, Schmid M. Kausch K, et al. Among authors: haaf t. Am J Med Genet. 1988 Oct;31(2):415-20. doi: 10.1002/ajmg.1320310221. Am J Med Genet. 1988. PMID: 3068990 Review.

3

Duplication 8q24.2----qter and 15q14----pter resulting from a 3:1 meiotic segregation of a maternal reciprocal translocation.

Kausch K, Haaf T, Schmid M. Kausch K, et al. Among authors: haaf t. Am J Med Genet. 1988 Dec;31(4):981-5. doi: 10.1002/ajmg.1320310433. Am J Med Genet. 1988. PMID: 3239587

4

Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2.

Zechner U, Scheel S, Hemberger M, Hopp M, Haaf T, Fundele R, Wanker EE, Lehrach H, Wedemeyer N, Himmelbauer H. Zechner U, et al. Among authors: haaf t. Genomics. 1998 Dec 15;54(3):505-10. doi: 10.1006/geno.1998.5584. Genomics. 1998. PMID: 9878254

5

Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes.

Wirth J, Nothwang HG, van der Maarel S, Menzel C, Borck G, Lopez-Pajares I, Brøndum-Nielsen K, Tommerup N, Bugge M, Ropers HH, Haaf T. Wirth J, et al. Among authors: haaf t. J Med Genet. 1999 Apr;36(4):271-8. J Med Genet. 1999. PMID: 10227392 Free PMC article.

6

Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?

Stout K, van der Maarel S, Frants RR, Padberg GW, Ropers HH, Haaf T. Stout K, et al. Among authors: haaf t. Chromosome Res. 1999;7(5):323-9. doi: 10.1023/a:1009287111661. Chromosome Res. 1999. PMID: 10515207

7

Two supernumerary marker chromosomes, originating from chromosomes 6 and 11, in a child with developmental delay and craniofacial dysmorphism.

Maurer B, Haaf T, Stout K, Reissmann N, Steinlein C, Schmid M. Maurer B, et al. Among authors: haaf t. Cytogenet Cell Genet. 2001;93(3-4):182-7. doi: 10.1159/000056982. Cytogenet Cell Genet. 2001. PMID: 11528110 Review.

8

Chicken microchromosomes are hypermethylated and can be identified by specific painting probes.

Grützner F, Zend-Ajusch E, Stout K, Munsche S, Niveleau A, Nanda I, Schmid M, Haaf T. Grützner F, et al. Among authors: haaf t. Cytogenet Cell Genet. 2001;93(3-4):265-9. doi: 10.1159/000056996. Cytogenet Cell Genet. 2001. PMID: 11528124

9

Elevated levels of Rad51 recombination protein in tumor cells.

Raderschall E, Stout K, Freier S, Suckow V, Schweiger S, Haaf T. Raderschall E, et al. Among authors: haaf t. Cancer Res. 2002 Jan 1;62(1):219-25. Cancer Res. 2002. PMID: 11782381

10

Plasticity of human chromosome 3 during primate evolution.

Tsend-Ayush E, Grützner F, Yue Y, Grossmann B, Hänsel U, Sudbrak R, Haaf T. Tsend-Ayush E, et al. Among authors: haaf t. Genomics. 2004 Feb;83(2):193-202. doi: 10.1016/j.ygeno.2003.08.012. Genomics. 2004. PMID: 14706448

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