1-Evaluation of relationship between chromosome 22 and p53 gene alterations and the subtype of meningiomas by the interphase-FISH technique. Yakut T, Bekar A, Doygun M, Acar H, Egeli U, Ogul E.Teratog Carcinog Mutagen. 2002;22(3):217-25. doi: 10.1002/tcm.
2-Comparison of genetic changes between interphase and metaphase nuclei in monitoring CML and APL treatment using DC-FISH technique. Yakut T, Ali R, Egeli U, Ozkalemkas F, Ercan I, Ozçelik T, Ozkocaman V, Yigit B, Tunali A.Cancer Biol Ther. 2004 Sep;3(9):
3-Investigation of c-myc and p53 gene alterations in the tumor and surgical borderline tissues of NSCLC and effects on clinicopathologic behavior: by the FISH technique.Yakut T, Egeli U, Gebitekin C.Lung. 2003;181(5):245-58. doi: 10.1007/s00408-003-1026-x
4-Toll-like receptor-9 gene polymorphism in common variable immunodeficiency. Tanir S, Karkucak M, Yakut T, Kilic SS.J Investig Allergol Clin Immunol. 2010;20(3):267-8.PMID: 20635795 Free article. No abstract available.
5-Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mende-lian Neurologic Disease.Karaca E, Harel T, Pehlivan D, Jhangiani SN, Gambin T, Coban Akdemir Z, Gonzaga-Jauregui C, Erdin S, Bayram Y, Campbell IM, Hunter JV, At
6-A fertile patient with 45X/47XXX mosaicism.Sahinturk S, Ozemri Sag S, Ture M, Gorukmez O, Topak A, Yakut T, Gulten T.Genet Couns. 2015;26(1):29-34.PMID: 26043504Cite
7-De novo partial trisomy distal 4q: a case report.Gorukmez O, Sag SO, Gorukmez O, Ture M, Gulten T, Yakut T.Genet Couns. 2014;25(4):423-8.PMID: 25804022
8-MMP2 gene-735 C/T and MMP9 gene -1562 C/T polymorphisms in JAK2V617F positive mye-loproliferative disorders.Sag SO, Gorukmez O, Ture M, Gorukmez O, Topak A, Sahinturk S, Ocakoglu G, Gulten T, Ali R, Yakut T.Asian Pac J Cancer Prev. 2015;16(2):443-9. doi
9-Dyskeratosis Congenita: A Case Report.Ozemri Sag S, Topak A, Gorukmez O, Gorukmez O, Ture M, Carrillo J, Sahinturk S, Gulten T, Perona R, Yakut T.Genet Couns. 2016;27(2):263-7.PMID: 29485835 No abstract available.
10-Meiotic segregation analysis of reciprocal translocations both in sperms and blastomeres.Yakut T, Ercelen N, Acar H, Kimya Y, Egeli U.Am J Med Genet A. 2006 May 15;140(10):1074-82. doi: 10.1002/ajmg.a.31215.PMID: 16596678
11-Association and Prognostic Significance of the Functional -1562C/T Polymorphism in the Promoter Region of MMP-9 in Turkish Patients with Gastric Cancer.Avcı N, Ture M, Deligonul A, Cubukcu E, Olmez OF, Sahinturk S,Topak A, Kurt E, Evrensel T, Şahin AB,
12-GSTT1 and GSTM1 gene polymorphisims in sarcoidosis.Coskun F, Karkucak M, Yilmaz D, Yakut T, Uzaslan E.Sarcoidosis Vasc Diffuse Lung Dis. 2016 Oct 7;33(3):253-257.PMID: 27758991
13-Delayed Puberty and Gonadal Failure in Patients with HAX1 Mutation.Cekic S, Saglam H, Gorukmez O, Yakut T, Tarim O, Kilic SS.J Clin Immunol. 2017 Aug;37(6):524-528. doi: 10.1007/s10875-017-0412-8. Epub 2017 Jul 5.PMID: 28681255
14-Investigation of MEFV gene polymorphisms (G138G and A165A) in adult patients with fami-lial Mediterranean fever.Öksuz MF, Karkucak M, Görukmez O, Ocakoğlu G, Yıldız A, Ture M, Yakut T, Dilek K.Rev Bras Reumatol Engl Ed. 2017 Nov-Dec;57(6):501-506. doi:
15-TURNER SYNDROME WITH 45,X/46,X,I(Xq)/47,X,I(Xq),I(Xq) KARYOTYPE.Gorukmez O, Sag SO, Gulten T, Gorukmez, Ture M, Yakut T.Genet Couns. 2015;26(2):267-9.PMID: 26349201 No abstract available.
16-Associations analysis of GSTM1, T1 and P1 Ile105Val polymorphisms with carpal tunnel synd-rome.Eroğlu P, Erkol İnal E, Sağ ŞÖ, Görükmez Ö, Topak A, Yakut T.Clin Rheumatol. 2016 May;35(5):1245-51. doi: 10.1007/s10067-014-2855-0. Epub 2015 Jan 9.PMID: 25
17-Association of GSTM1, GSTT1, GSTP1-ILE105VAL and ACE I/D polymorphisms with ankylosing spondylitis.İnal EE, Görükmez O, Eroğlu S, Görükmez Ö, Solak Ö, Topak A, Yakut T.Rheumatol Int. 2016 Jan;36(1):17-23. doi: 10.1007/s00296-015-3317-y. Epub 2015 Jul 1
18-Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis.Ceylan E, Karkucak M, Coban H, Karadag M, Yakut T.J Infect Public Health. 2017 Nov-Dec;10(6):774-777. doi: 10.1016/j.jiph.2016.11.003. Epub
19-Association between the catechol-o-methyltransferase val158met polymorphism with sus-ceptibility and severity of carpal tunnel syndrome.Erkol İnal E, Eroğlu P, Görükmez O, Özemri Sağ Ş, Yakut T.Balkan J Med Genet. 2016 Jul 9;18(2):43-48. doi: 10.1515/b
20-Distribution of KRAS and BRAF Mutations in Metastatic Colorectal Cancers in Turkish Pati-ents.Gorukmez O, Yakut T, Gorukmez O, Sag SO, Karkucak M, Kanat O.Asian Pac J Cancer Prev. 2016;17(3):1175-9. doi: 10.7314/apjcp.2016.17.3.1175.PMID: 27039744 Free
21-CLINICAL EFFECT OF A MUTATION (p.Glu322Asp, c.966 G>T) IN PANK2 GENE IN A FAMILY WITH ATYPICAL PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION.Ayas ZO, Karkucak M, Ocal RO, Yakut T.Genet Couns. 2016;27(4):489-494.PMID: 30226968
22-Glutathione S-transferase T1, M1 and P1 Genetic Polymorphisms and Susceptibility to Colo-rectal Cancer in Turkey.Gorukmez O, Yakut T, Gorukmez O, Sag SO, Topak A, Sahinturk S, Kanat O.Asian Pac J Cancer Prev. 2016;17(8):3855-9.PMID: 27644629 Free artic
23-Glutathione S-Transferase M1 and T1 Gene Polymorphisms in Patients with Chronic Plaque-Type Psoriasis: A Case-Control Study.Solak B, Karkucak M, Turan H, Ocakoğlu G, Özemri Sağ Ş, Uslu E, Yakut T, Erdem T.Med Princ Pract. 2016;25(2):155-8. doi: 10.1159
24Spectrum of EGFR gene mutations and ALK rearrangements in lung cancer patients in Turkey.Sag SO, Gorukmez O, Ture M, Gorukmez O, Deligonul A, Sahinturk S, Topak A, Gulten T, Kurt E, Yakut T.Springerplus. 2016 Apr 19;5:482. doi: 10.1186/s40064-016-2150-4
25-Oxytocin system social function impacts in children with attention-deficit/hyperactivity di-sorder.Ayaz AB, Karkucak M, Ayaz M, Gokce S, Kayan E, Güler EE, Güngen BD, Kuşcu TD, Ocakoğlu G, Yakut T.Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):
26-The Effects of Bundles on Catheter-Associated Urinary Tract Infections in the Pediatric Inten-sive Care Unit.Sönmez Düzkaya D, Bozkurt G, Uysal G, Yakut T.Clin Nurse Spec. 2016 Nov/Dec;30(6):341-346. doi: 10.1097/NUR.0000000000000246.PMID: 27753672
27-The Effect of Oral Care Using an Oral Health Care Guide on Preventing Mucositis in Pediat-ric Intensive Care.Düzkaya DS, Uysal G, Bozkurt G, Yakut T.J Pediatr Nurs. 2017 Sep-Oct;36:98-102. doi: 10.1016/j.pedn.2017.05.010. Epub 2017 Jun 3.PMID: 28888518
28-Severe hypospadias associated with Robertsonian translocation.Kilic N, Balkan E, Saglam H, Yakut T, Dogruyol H.Urol Int. 2005;74(4):373-6. doi: 10.1159/000084443.PMID: 15897709
29-Reanalysis of human blastocysts with different molecular genetic screening platforms reve-als significant discordance in ploidy status.Tortoriello DV, Dayal M, Beyhan Z, Yakut T, Keskintepe L.J Assist Reprod Genet. 2016 Nov;33(11):1467-1471. doi: 10.10
30-The Influence of Polymorphisms of Interleukin-17A and -17F Genes on Susceptibility and Ac-tivity of Rheumatoid Arthritis.Erkol İnal E, Görükmez O, Dündar Ü, Görükmez Ö, Yener M, Özemri Sağ Ş, Yakut T.Genet Test Mol Biomarkers. 2015 Aug;19(8):461-4. doi
31-Associations between polymorphisms of IL-17F and IL-17A genes with disease activity and clinical outcome of Ankylosing Spondylitis.Erkol İnal E, Görükmez O, Eroğlu S, Özemri SŞ, Solak Ö, Görükmez Ö, Yakut T.Acta Reumatol Port. 2016 Jul-Sep;41(3):232-23
32-The variant translocation of ABL1 gene t(2;9)(q21;q34) in a childhood T-cell acute lymphob-lastic leukemia.Karkucak M, Yakut T, Baytan B, Gulten T, Gunes AM.Bratisl Lek Listy. 2012;113(1):19-20. doi: 10.4149/bll_2012_004.PMID: 22380496
33-Association of the ACE I/D gene polymorphisms with JAK2V617F-positive polycythemia vera and essential thrombocythemia.Karkucak M, Yakut T, Baytan B, Gulten T, Gunes AM.Bratisl Lek Listy. 2012;113(1):19-20. doi: 10.4149/bll_2012_004.PMID: 22380496
34-Does MBL2 codon 54 polymorphism play a role in the pathogenesis of psoriasis?Turan H, Karkucak M, Yakut T, Ozsahin M, Gurlevik Z, Yanik ME, Ucgun T, Aliagaoglu C, Yaykasli KO.Int J Dermatol. 2014 Jan;53(1):34-8. doi: 10.1111/j.1365-4632.2012.5657.x. Ep
35-Association between p16(CDKN2A) C540G polymorphism and tumor behavior in prolactino-ma: A single-center study.Cander S, Karkucak M, Gul OO, Sag SO, Yakut T, Ersoy C, Tuncel E, Erturk E.Biomed Rep. 2014 Jul;2(4):589-595. doi: 10.3892/br.2014.281. Epub 2
36-Esophageal muscle cell interaction with biopolymers.Korkmaz M, Yakut T, Narci A, Güvenç BH, Güilten T, Yağmurca M, Yiğit B, Bilir A.Med Sci Mo-nit. 2007 Feb;13(2):BR46-9.PMID: 17261980
37-A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.Tatar A, Oztas S, Yakut T, Ors R.Genet Couns. 2005;16(2):173-7.PMID: 16080298
38-Effect of cyclin [corrected] D1 (CCND1) gene polymorphism on tumor formation and beha-vior in patients with prolactinoma.Cander S, Ertürk E, Karkucak M, Oz Gül O, Görükmez O, Yakut T, Unal OK, Ersoy C, Tuncel E, Imamoğlu S.Gene. 2012 Nov 1;509(1):158-6
39-Cathecol-O-methyl transferase Val158Met genotype is not a risk factor for conversion disor-der.Armagan E, Almacıoglu ML, Yakut T, Köse A, Karkucak M, Köksal O, Görükmez O.Genet Mol Res. 2013 Mar 19;12(1):852-8. doi: 10.4238/2013.March.19.1.PMID: 236131
40-Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malforma-tions.Rainger J, Pehlivan D, Johansson S, Bengani H, Sanchez-Pulido L, Williamson KA, Ture M, Barker H, Rosendahl K, Spranger J, Horn D, Meynert A, Floyd JA, Prescott
41-Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods.Ozemri Sag S, Yakut T, Gorukmez O, Gorukmez O, Ture M, Karkucak M, Gulten T, Ali R.Ge
42-ACE gene I/D polymorphism and risk of sarcoidosis development in Turkish patients.Yılmaz D, Karkucak M, Coşkun F, Yakut T, Kunt Uzaslan E.Tuberk Toraks. 2012;60(3):201-6. doi: 10.5578/tt.3935.PMID: 23030744 Free article.
43-Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential throm-bocythemia and polycythemia vera.Karkucak M, Yakut T, Ozkocaman V, Ozkalemkas F, Ali R, Bayram M, Gorukmez O, Ocakoglu G.Mol Biol Rep. 2012 Sep;39(9):8663-7. doi: 10.10
44-A novel mutation in the FRAS1 gene in a patient with Fraser syndrome.Ozemri Sag S, Gorukmez O, Gorukmez O, Ture M, Sahinturk S, Topak A, Gulten T, Schanze D, Yakut T, Zenker M.Genet Couns. 2015;26(1):21-7.PMID: 26043503
45-A RARE COMBINATION OF 45,X/46,XY MOSAICISM AND Y CHROMOSOME MICRODELETION IN AN INFERTILE MAN WITH AZOOSPERMIA.Aydemir H, Karkucak M, Cimen HI, Halis F, Kumsar S, Sonbahar AE, Yakut T.Genet Couns. 2016;27(1):95-8.PMID: 27192898 No abstract available.
46-An Unusual Case of LCHAD Deficiency Presenting With a Clinical Picture of Hemophagocytic Lymphohistiocytosis: Secondary HLH or Coincidence?Erdol S, Ture M, Baytan B, Yakut T, Saglam H.J Pediatr Hematol Oncol. 2016 Nov;38(8):661-662. doi: 10.1097/MPH.00
47-Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroi-dism.Cangul H, Morgan NV, Forman JR, Saglam H, Aycan Z, Yakut T, Gulten T, Tarim O, Bober E, Ce-sur Y, Kirby GA, Pasha S, Karkucak M, Eren E, Cetinkaya S, Bas V, Dem
48-A NOVEL MUTATION IN NPR2 GENE IN A PATIENT WITH ACROMESOMELIC DYSPLASIA, MA-ROTEAUX TYPE.Sag SO, Gorukmez O, Topak A, Gorukmez O, Ture M, Sahinturk S, Gulten T, Yakut T.Genet Co-uns. 2015;26(2):219-25.PMID: 26349192 Orhan O, Atalay MA, Orhan F, Karkuca
50-Investigation of TNF-alpha gene (G308A) and GSTP1 gene (Ilel05Val) polymorphisms in Tur-kish patients with retinopathy of prematurity.Türe M, Yildiz M, Karkucak M, Gülten ET, Siğirli D, Özmen AT, Yakut T.Turk J Med Sci. 2015;45(1):164-9. doi: 10.3906/s
51-Vitamin a deficiency in patients with common variable immunodeficiency.Kilic SS, Kezer EY, Ilcol YO, Yakut T, Aydin S, Ulus IH.J Clin Immunol. 2005 May;25(3):275-80. doi: 10.1007/s10875-005-4090-6.PMID: 15981093
52-Comparison of aneuploidy frequencies between in vitro matured and unstimulated cycles oocytes by metaphase comparative genomic hybridization (mCGH).Yakut T, Karkucak M, Sher G, Keskintepe L.Mol Biol Rep. 2012 May;39(5):6187-91. doi: 10.1007/s11033-011-
53-MULTIPLE CONGENITAL ANOMALIES IN A CHILD WITH 47,XY,+der(8;9)(p10;p10): A CASE REPORT.Gorukmez O, Gorukmez O, Sag OS, Yakut T, Gulten T.Genet Couns. 2015;26(2):163-9.PMID: 26349185
54-Polymorphisms of glutathione-s-transferase M1, T1, and P1 genes in endometrial carcino-ma.Ozerkan K, Atalay MA, Yakut T, Doster Y, Yilmaz E, Karkucak M.Eur J Gynaecol Oncol. 2013;34(1):42-7.PMID: 23589999
55-FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.Yakut T, Kilic SS, Cil E, Yapici E, Egeli U.Pediatr Surg Int. 2006 Apr;22(4):380-3. doi: 10.1007/s00383-006-1641-8. Epub 2006 Feb 4.PMID: 16463032
56-GST (GSTM1, GSTT1, and GSTP1) polymorphisms in the genetic susceptibility of Turkish pati-ents to cervical cancer.Kiran B, Karkucak M, Ozan H, Yakut T, Ozerkan K, Sag S, Ture M.J Gynecol Oncol. 2010 Sep;21(3):169-73. doi: 10.3802/jgo.2010.21.3.169. Epu
57-Investigation of Monnose-Binding Lectin gene Polymorphism in Patients with Erythema Mul-tiforme, Stevens-Johnson Syndrome and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Overlap SyKarkucak M, Bülbül EB, Turan H, Yakut T, Toka S, Sarıcaoğlu H.Ba
58-Investigation of ABCB1 gene polymorphism with colchicine response in Behçet's disease.Saricaoglu H, Yilmaz M, Karkucak M, Ozturk HZ, Yakut T, Gulten T, Baskan EB, Aydogan K, Dilek K.Genet Mol Res. 2011 Jan 4;10(1):1-6. doi: 10.4238/vol10-1gmr824.PMID:
59-The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels.Sogutlu Sari E, Yazici A, Eser B, Erol MK, Kilic A, Ermis SS, Koytak A, Akşit H, Yak
60-Assessment of molecular events in squamous and non-squamous cell lung carcinoma.Yakut T, Schulten HJ, Demir A, Frank D, Danner B, Egeli U, Gebitekin C, Kahler E, Gunawan B, Urer N, Oztürk H, Füzesi L.Lung Cancer. 2006 Dec;54(3):293-301. doi: 10.1016/j.
61-Frequency of recombinant and nonrecombinant products of pericentric inversion of chromo-some 1 in sperm nuclei of carrier: by FISH technique.Yakut T, Acar H, Egeli U, Kimya Y.Mol Reprod Dev. 2003 Sep;66(1):67-71. doi: 10.1002/mrd.10325.PMID: 12874801
62-Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures.Yildiz M, Karkucak M, Yakut T, Gorukmez O, Ozmen A.Genet Mol Res. 2010 Oct 26;9(4):2131
63-Effect of Pressure Injury Prevention Guides Used In a Pediatric Intensive Care.Uysal G, Sönmez Düzkaya D, Yakut T, Bozkurt G.Clin Nurs Res. 2020 May;29(4):249-255. doi: 10.1177/1054773818817696. Epub 2019 Jan 2.PMID: 30599767
64-NOVEL MUTATION OF THE ELECTRON TRANSFERRING FLAVOPROTEIN DEHYDROGENASE (ETFDH) GENE IN THE ISOLATED MYOPATHIC FORM OF COENZYME q10 DEFICIENCY.Gorukmez O, Gorukmez O, Sag SO, Erdol S, Saglam H, Yakut T.Genet Couns. 2015;26(2):259-62.PMID: 26349199 No ab
65-Recurrence of Oligodendroglioma Remote From the Original Site: A Case ReportKocaeli H, Yakut T, Bekar A, Taşkapilioğlu O, Tolunay S.Surg Neurol. 2006 Dec;66(6):627-30; discussion 630-1. doi: 10.1016/j.surneu.2006.02.049. Epub 2006 Oct . 6.PMID: 1714533
66-Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome.Turan H, Bulbul Baskan E, Yakut T, Karkucak M, Tunali S, Saricaoglu H.Bratisl Lek
67-Correlation of chromosomal imbalances by comparative genomic hybridization and expres-sion of EGFR, PTEN, p53, and MIB-1 in diffuse gliomas.Yakut T, Gutenberg A, Bekar A, Egeli U, Gunawan B, Ercan I, Tolunay S, Doygun M, Schulten HJ.Oncol Rep. 2007 May
68-Oocyte karyotyping by comparative genomic hybridization [correction of hybrydization] pro-vides a highly reliable method for selecting "competent" embryos, markedly improving in vitro fertilization outcome: a multiphase study.
69-Sher G, Keskintepe L, Keskintepe M, Ginsburg M, Maassarani G, Yakut T, Baltaci V, Kotze D, Unsal E.Fertil Steril. 2007 May;87(5):1033-40. doi: 10.1016/j.fertnstert.2006.08.108. Epub 2007 Jan 29.PMID: 17258713
70-Pregnancy under treatment of imatinib and successful labor in a patient with chronic mye-logenous leukemia (CML). Outcome of discontinuation of imatinib therapy after achieving a molecular remission.Ali R, Ozkalemkaş F, Ozçelik T, Ozkocaman V, Ozan U,
71-Cytogenetic results of amniocentesis materials: incidence of abnormal karyotypes in the Turkish collaborative study.Karaoguz MY, Bal F, Yakut T, Ercelen NO, Ergun MA, Gokcen AB, Biri AA, Kimya Y, Urman B, Gultomruk M, Egeli U, Menevse S.Genet Couns. 20
72-Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mu-tation at the SOX9 locus.Temel SG, Gulten T, Yakut T, Saglam H, Kilic N, Bausch E, Jin WJ, Leipoldt M, Scherer G.Sex Dev. 2007;1(1):24-34. doi: 10.1159/000096236
73-Sudden blastic crisis and additional chromosomal abnormalities during chronic myeloid leu-kemia in the imatinib era.Ali R, Ozkalemkas F, Ozkocaman V, Yakut T, Nazlioglu HO, Budak F, Pekgoz M, Korkmaz S, Kar-kucak M, Ozcelik T, Tunali A.Int J Clin Oncol
74-Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.Kímya Y, Yakut T, Egelí U, Ozerkan K.Prenat Diagn. 2002 Nov;22(11):957-61. doi: 10.1002/pd.403.PMID: 12424755
75-Another small supernumerary marker chromosome derived from chromosome 9 in a Kline-felter patient.Gulten T, Gorukmez O, Gorukmez O, Karkucak M, Ture M, Yakut T.West Indian Med J. 2012 Dec;61(9):924-7. doi: 10.7727/wimj.2012.027.PMID: 24020236
76-Low frequency of p53 and k-ras codon 12 mutations in non-small cell lung carcinoma (NSCLC) tumors and surgical margins.Vatan O, Bilaloglu R, Tunca B, Cecener G, Gebitekin C, Egeli U, Yakut T, Urer N.Tumori. 2007 Sep-Oct;93(5):473-7.PMID: 18038880
77-Impact of concomitant obstructive sleep apnea on pulmonary involvement and main pulmo-nary artery diameter in adults with scleroderma.Yakut T, Balcan B, Karakurt S, Direskeneli H, Yalcinkaya Y, Peker Y.Sleep Breath. 2020 Apr 13. doi: 10.1007/s11325-020
78-Determination of allelic deletion of multiple endocrine neoplasm type 1 (MEN1) gene in acute myeloid leukemia (AML) by application of FISH-TSA technique.Acar H, Kaynak M, Yakut T, Uçar F, Egeli U.Teratog Carcinog Mutagen. 2002;22(5):369-75. doi: 10.100
79-Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene.Cangül H, Ozdemir O, Yakut T, Okan M, Morgan NV, Baytan B, Kurian MA, Spiegel R,
80-Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients.Yakut T, Karkucak M, Ursavas A, Gulten T, Burgazlioglu B, Gorukmez O, Karadag M.Genet Mol Res. 2010 Apr 20;9(2):734-8. doi: 10.4238/vol9-2gmr755.
81-AML1 amplification and 17q25 deletion in a case of childhood acute lymphoblastic leuke-mia.Gulten T, Yakut T, Karkucak M, Baytan B, Guneş AM.J Clin Lab Anal. 2009;23(6):368-71. doi: 10.1002/jcla.20343.PMID: 19927343 Free PMC article.
