Yakut S - Search Results

1

Aberrations of chromosomes 9 and 22 in acute lymphoblastic leukemia cases detected by ES-fluorescence in situ hybridization.

Cetin Z, Yakut S, Karadogan I, Kupesiz A, Timuragaoglu A, Salim O, Tezcan G, Alanoglu G, Ozbalci D, Hazar V, Yesilipek MA, Undar L, Luleci G, Berker S. Cetin Z, et al. Among authors: yakut s. Genet Test Mol Biomarkers. 2012 May;16(5):318-23. doi: 10.1089/gtmb.2011.0186. Epub 2012 Feb 23. Genet Test Mol Biomarkers. 2012. PMID: 22360868

2

Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12.

Cetin Z, Mihci E, Yakut S, Keser I, Karauzum SB, Luleci G. Cetin Z, et al. Among authors: yakut s. Am J Med Genet A. 2011 Feb;155A(2):349-52. doi: 10.1002/ajmg.a.33811. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271652

3

A patient with Down syndrome with a de novo derivative chromosome 21.

Cetin Z, Yakut S, Mihci E, Manguoglu AE, Berker S, Keser I, Luleci G. Cetin Z, et al. Among authors: yakut s. Gene. 2012 Oct 10;507(2):159-64. doi: 10.1016/j.gene.2012.07.018. Epub 2012 Jul 22. Gene. 2012. PMID: 22827956

4

Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia.

Yakut S, Cetin Z, Clark OA, Usta MF, Berker S, Luleci G. Yakut S, et al. Gene. 2013 Jan 1;512(1):157-60. doi: 10.1016/j.gene.2012.09.063. Epub 2012 Sep 29. Gene. 2013. PMID: 23031811

5

A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.

Cetin Z, Yakut S, Clark OA, Mihci E, Berker S, Luleci G. Cetin Z, et al. Among authors: yakut s. Gene. 2013 Mar 1;516(1):176-80. doi: 10.1016/j.gene.2012.12.013. Epub 2012 Dec 20. Gene. 2013. PMID: 23262338

6

Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages.

Yakut S, Berker-Karaüzüm S, Simşek M, Zorlu G, Trak B, Lüleci G. Yakut S, et al. Clin Genet. 2002 Jan;61(1):26-31. doi: 10.1034/j.1399-0004.2002.610105.x. Clin Genet. 2002. PMID: 11903351

7

Novel cytogenetic findings revealed by conventional cytogenetic and FISH analyses in leukaemia patients.

Karauzum SB, Bilgen T, Karadogan I, Yakut S, Cetin Z, Ugur A, Luleci G. Karauzum SB, et al. Among authors: yakut s. Exp Oncol. 2005 Sep;27(3):229-32. Exp Oncol. 2005. PMID: 16244587

8

M-FISH applications in clinical genetics.

Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G. Cetin Z, et al. Among authors: yakut s. Genet Couns. 2005;16(3):257-68. Genet Couns. 2005. PMID: 16259323

9

Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16.

Yakut S, Cetin Z, Simşek M, Karaüzüm SB, Tükün A, Lüleci G. Yakut S, et al. Genet Couns. 2009;20(4):327-32. Genet Couns. 2009. PMID: 20162867

10

De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.

Yakut S, Cetin Z, Berker-Karauzum S, Mihci E, Mendilcioglu I, Luleci G. Yakut S, et al. Genet Couns. 2011;22(1):63-8. Genet Couns. 2011. PMID: 21614990

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