Tumer Z - Search Results

1

Metaphase FISH on a chip: miniaturized microfluidic device for fluorescence in situ hybridization.

Vedarethinam I, Shah P, Dimaki M, Tumer Z, Tommerup N, Svendsen WE. Vedarethinam I, et al. Among authors: tumer z. Sensors (Basel). 2010;10(11):9831-46. doi: 10.3390/s101109831. Epub 2010 Nov 2. Sensors (Basel). 2010. PMID: 22163442 Free PMC article.

2

Advanced microtechnologies for detection of chromosome abnormalities by fluorescent in situ hybridization.

Kwasny D, Vedarethinam I, Shah P, Dimaki M, Silahtaroglu A, Tumer Z, Svendsen WE. Kwasny D, et al. Among authors: tumer z. Biomed Microdevices. 2012 Jun;14(3):453-60. doi: 10.1007/s10544-011-9622-7. Biomed Microdevices. 2012. PMID: 22222279 Review.

3

Centrifugally driven microfluidic disc for detection of chromosomal translocations.

Brøgger AL, Kwasny D, Bosco FG, Silahtaroglu A, Tümer Z, Boisen A, Svendsen WE. Brøgger AL, et al. Among authors: tumer z. Lab Chip. 2012 Nov 21;12(22):4628-34. doi: 10.1039/c2lc40554g. Lab Chip. 2012. PMID: 22911443

4

Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.

Sogaard M, Tümer Z, Hjalgrim H, Hahnemann J, Friis B, Ledaal P, Pedersen VF, Baekgaard P, Tommerup N, Cingöz S, Duno M, Brondum-Nielsen K. Sogaard M, et al. Among authors: tumer z. BMC Med Genet. 2005 May 17;6:21. doi: 10.1186/1471-2350-6-21. BMC Med Genet. 2005. PMID: 15904506 Free PMC article.

5

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

6

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.

7

Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features.

Sehested LT, Møller RS, Bache I, Andersen NB, Ullmann R, Tommerup N, Tümer Z. Sehested LT, et al. Among authors: tumer z. Am J Med Genet A. 2010 Dec;152A(12):3115-9. doi: 10.1002/ajmg.a.33476. Am J Med Genet A. 2010. PMID: 21082657

8

Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation.

Gilling M, Lind-Thomsen A, Mang Y, Bak M, Møller M, Ullmann R, Kristoffersson U, Kalscheuer VM, Henriksen KF, Bugge M, Tümer Z, Tommerup N. Gilling M, et al. Among authors: tumer z. Eur J Med Genet. 2011 Jul-Aug;54(4):e383-8. doi: 10.1016/j.ejmg.2011.03.008. Epub 2011 Mar 21. Eur J Med Genet. 2011. PMID: 21426945

9

Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome.

Boonen SE, Stahl D, Kreiborg S, Rosenberg T, Kalscheuer V, Larsen LA, Tommerup N, Brøndum-Nielsen K, Tümer Z. Boonen SE, et al. Among authors: tumer z. Am J Med Genet A. 2005 Jan 30;132A(3):324-8. doi: 10.1002/ajmg.a.30422. Am J Med Genet A. 2005. PMID: 15690381 Review.

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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