Tümer Z - Search Results

1

Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.

Belloso JM, Bache I, Guitart M, Caballin MR, Halgren C, Kirchhoff M, Ropers HH, Tommerup N, Tümer Z. Belloso JM, et al. Among authors: tumer z. Eur J Hum Genet. 2007 Jun;15(6):711-3. doi: 10.1038/sj.ejhg.5201824. Epub 2007 Mar 28. Eur J Hum Genet. 2007. PMID: 17392702

2

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.

Tümer Z, Chelly J, Tommerup N, Ishikawa-Brush Y, Tønnesen T, Monaco AP, Horn N. Tümer Z, et al. Hum Mol Genet. 1992 Oct;1(7):483-9. doi: 10.1093/hmg/1.7.483. Hum Mol Genet. 1992. PMID: 1307248

3

Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2.

Tümer Z, Tommerup N, Tønnesen T, Kreuder J, Craig IW, Horn N. Tümer Z, et al. Hum Genet. 1992 Mar;88(6):668-72. doi: 10.1007/BF02265295. Hum Genet. 1992. PMID: 1348049

4

Assignment of the human gene for pregnancy-associated plasma protein A (PAPPA) to 9q33.1 by fluorescence in situ hybridization to mitotic and meiotic chromosomes.

Silahtaroglu AN, Tümer Z, Kristensen T, Sottrup-Jensen L, Tommerup N. Silahtaroglu AN, et al. Among authors: tumer z. Cytogenet Cell Genet. 1993;62(4):214-6. doi: 10.1159/000133479. Cytogenet Cell Genet. 1993. PMID: 7679961

5

Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric alpha-satellite sequences.

Tümer Z, Berg A, Mikkelsen M. Tümer Z, et al. Hum Genet. 1995 Mar;95(3):299-302. doi: 10.1007/BF00225197. Hum Genet. 1995. PMID: 7868122

6

A cytogenetic survey in Menkes disease: implications for the detection of chromosomal rearrangements in X linked disorders.

Tommerup N, Tümer Z, Tønnesen T, Horn N. Tommerup N, et al. Among authors: tumer z. J Med Genet. 1993 Apr;30(4):314-5. doi: 10.1136/jmg.30.4.314. J Med Genet. 1993. PMID: 8487278 Free PMC article. No abstract available.

7

Not para-, not peri-, but centric inversion of chromosome 12.

Silahtaroglu AN, Hacihanefioglu S, Güven GS, Cenani A, Wirth J, Tommerup N, Tümer Z. Silahtaroglu AN, et al. Among authors: tumer z. J Med Genet. 1998 Aug;35(8):682-4. doi: 10.1136/jmg.35.8.682. J Med Genet. 1998. PMID: 9719380 Free PMC article.

8

Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome.

Silahtaroglu A, Hol FA, Jensen PK, Erdel M, Duba HC, Geurds MP, Knoers NV, Mariman EC, Tümer Z, Utermann G, Wirth J, Bugge M, Tommerup N. Silahtaroglu A, et al. Among authors: tumer z. Eur J Hum Genet. 1999 Jan;7(1):68-76. doi: 10.1038/sj.ejhg.5200260. Eur J Hum Genet. 1999. PMID: 10094193

9

Assignment of the human zinc finger gene, ZNF288, to chromosome 3 band q13.2 by radiation hybrid mapping and fluorescence in situ hybridisation.

Harboe TL, Tümer Z, Hansen C, Jensen NA, Tommerup N. Harboe TL, et al. Among authors: tumer z. Cytogenet Cell Genet. 2000;89(3-4):156-7. doi: 10.1159/000015600. Cytogenet Cell Genet. 2000. PMID: 10965110 No abstract available.

10

Assignment of the NR2E3 gene to mouse chromosome 9 and to human chromosome 15q22.33-->q23.

Rendtorff ND, Vissing H, Tümer Z, Silahtaroglu A, Tommerup N. Rendtorff ND, et al. Among authors: tumer z. Cytogenet Cell Genet. 2000;89(3-4):279-80. doi: 10.1159/000015635. Cytogenet Cell Genet. 2000. PMID: 10965145 No abstract available.

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