Tümer Z - Search Results

1

A human phenome-interactome network of protein complexes implicated in genetic disorders.

Lage K, Karlberg EO, Størling ZM, Olason PI, Pedersen AG, Rigina O, Hinsby AM, Tümer Z, Pociot F, Tommerup N, Moreau Y, Brunak S. Lage K, et al. Among authors: tumer z. Nat Biotechnol. 2007 Mar;25(3):309-16. doi: 10.1038/nbt1295. Nat Biotechnol. 2007. PMID: 17344885 Free article.

2

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

3

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

4

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.

5

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.

6

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.

7

Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS).

Silahtaroglu AN, Brondum-Nielsen K, Gredal O, Werdelin L, Panas M, Petersen MB, Tommerup N, Tümer Z. Silahtaroglu AN, et al. Among authors: tumer z. BMC Genet. 2002 Apr 19;3:5. doi: 10.1186/1471-2156-3-5. BMC Genet. 2002. PMID: 11991808 Free PMC article.

8

Genomic structure, chromosome mapping and expression analysis of the human AVIL gene, and its exclusion as a candidate for locus for inflammatory bowel disease at 12q13-14 (IBD2).

Tümer Z, Croucher PJ, Jensen LR, Hampe J, Hansen C, Kalscheuer V, Ropers HH, Tommerup N, Schreiber S. Tümer Z, et al. Gene. 2002 Apr 17;288(1-2):179-85. doi: 10.1016/s0378-1119(02)00478-x. Gene. 2002. PMID: 12034507

9

Identification of a novel EYA1 splice-site mutation in a Danish branchio-oto-renal syndrome family.

Henriksen AM, Tümer Z, Tommerup N, Tranebjaerg L, Larsen LA. Henriksen AM, et al. Among authors: tumer z. Genet Test. 2004 Winter;8(4):404-6. doi: 10.1089/gte.2004.8.404. Genet Test. 2004. PMID: 15684871

10

Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease.

Baekvad-Hansen M, Tümer Z, Delicado A, Erdogan F, Tommerup N, Larsen LA. Baekvad-Hansen M, et al. Among authors: tumer z. Am J Med Genet A. 2006 Mar 1;140(5):427-33. doi: 10.1002/ajmg.a.31087. Am J Med Genet A. 2006. PMID: 16470726

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