Tarkan Argüden Y - Search Results

1

t(1;3)(p36;p21): presentation of a patient with MDS/AML (M2) and review of the literature.

Güven GS, Tarkan Argüden Y, Öngören Ş, Deviren A, Aydın Y, Hacıhanefioglu S. Güven GS, et al. Among authors: tarkan arguden y. Turk J Haematol. 2006 Jun 5;23(2):115-8. Turk J Haematol. 2006. PMID: 27265294 English.

2

Variant Philadelphia translocations with different breakpoints in six chronic myeloid leukemia patients.

Kuru D, Tarkan Argüden Y, Ar MC, Çırakoğlu A, Öngören Ş, Yılmaz Ş, Eşkazan AE, Deviren A, Soysal T, Hacıhanefioğlu S, Ülkü B. Kuru D, et al. Among authors: tarkan arguden y. Turk J Haematol. 2011 Sep 5;28(3):186-92. doi: 10.5152/tjh.2011.52. Turk J Haematol. 2011. PMID: 27264365 Free article. English.

3

A childhood acute lymphoblastic leukemia (ALL) case with t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12).

Kuru D, Yılmaz F, Berra SG, Canpolat C, Hacıhanefioğlu S, Tarkan Argüden Y, Deviren A, Çırakoğlu A. Kuru D, et al. Among authors: tarkan arguden y. Turk J Haematol. 2008 Sep 5;25(3):152-4. Turk J Haematol. 2008. PMID: 27264709 English.

4

Recurrent Monosomies Confirmed by Interphase FISH in Three Chronic Myeloid Leukemia Cases.

Tarkan Argüden Y, Kuru D, Çırakoğlu A, Yılmaz Ş, Öngören Aydın Ş, Ar CM, Deviren A, Soysal T, Hacıhanefioğlu S. Tarkan Argüden Y, et al. Turk J Haematol. 2015 Mar 5;32(1):82-4. doi: 10.4274/tjh.2014.0374. Turk J Haematol. 2015. PMID: 25805682 Free PMC article. No abstract available.

5

Supernumerary chromosome der(22)t(11;22): Emanuel syndrome associates with novel features.

Yosunkaya Fenerci E, Guven GS, Kuru D, Yilmaz S, Tarkan-Argüden Y, Cirakoglu A, Deviren A, Yüksel A, Hacihanefioğlu S. Yosunkaya Fenerci E, et al. Among authors: tarkan arguden y. Genet Couns. 2007;18(4):401-8. Genet Couns. 2007. PMID: 18286821

6

Mosaic supernumerary r(8) syndrome.

Yilmaz S, Tarkan-Argüden Y, Kuru D, Deviren A, Karaman B, Yüksel A, Hacihanefioğlu S. Yilmaz S, et al. Among authors: tarkan arguden y. Genet Couns. 2005;16(2):187-90. Genet Couns. 2005. PMID: 16080301 No abstract available.

7

A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analysis.

Akçakaya NH, Salman B, Görmez Z, Tarkan Argüden Y, Çırakoğlu A, Çakmur R, Dönmez Çolakoğlu B, Hacıhanefioğlu S, Özbek U, Yapıcı Z, Uğur İşeri SA. Akçakaya NH, et al. Among authors: tarkan arguden y. Neuromolecular Med. 2019 Mar;21(1):54-59. doi: 10.1007/s12017-018-08522-6. Epub 2019 Jan 5. Neuromolecular Med. 2019. PMID: 30612247

8

3p abnormalities in peripheral lymphocytes in small cell lung cancer.

Tarkan-Argüden Y, Hacihanefioglul S, Ongen G, Erk M, Cenani A. Tarkan-Argüden Y, et al. Tumori. 2009 Jul-Aug;95(4):535-7. doi: 10.1177/030089160909500423. Tumori. 2009. PMID: 19856671

9

Are monosomies underestimated while analyzing cancer cells?

Tarkan-Argüden Y. Tarkan-Argüden Y. Exp Oncol. 2009 Dec;31(4):194. Exp Oncol. 2009. PMID: 20010536 No abstract available.

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