Keser I - Search Results

1

Two rare mutations in Turkey: IVS I.130(G-C) and IVS II.848(C-A).

Nal N, Manguoglu AE, Sargin CF, Keser I, Kupesiz A, Yesilipek A, Luleci G. Nal N, et al. Among authors: keser i. Clin Lab Haematol. 2005 Aug;27(4):274-7. doi: 10.1111/j.1365-2257.2005.00691.x. Clin Lab Haematol. 2005. PMID: 16048497

2

Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya.

Keser I, Sanlioglu AD, Manguoglu E, Guzeloglu Kayisli O, Nal N, Sargin F, Yesilipek A, Simsek M, Mendilcioglu I, Canatan D, Luleci G. Keser I, et al. Acta Haematol. 2004;111(4):205-10. doi: 10.1159/000077567. Acta Haematol. 2004. PMID: 15153712

3

Hb Antalya [codons 3-5 (Leu-Thr-Pro-->Ser-Asp-Ser)]: a new unstable variant leading to chronic microcytic anemia and high Hb A2.

Keser I, Kayisli OG, Yesilipek A, Ozes ON, Luleci G. Keser I, et al. Hemoglobin. 2001 Nov;25(4):369-73. doi: 10.1081/hem-100107873. Hemoglobin. 2001. PMID: 11791869

4

The phenotypic effect of Hb G-Coushatta [beta22 (B4) Glu-Ala] and association with IVS.II.1(G-A) in a Turkish family.

Sargin CF, Nal N, Manguoglu AE, Keser I, Mendilcioglu I, Yesilipek A, Luleci G. Sargin CF, et al. Among authors: keser i. Genet Couns. 2005;16(3):307-8. Genet Couns. 2005. PMID: 16259329 No abstract available.

5

Frequencies of four genetic polymorphisms in the CYP1A2 gene in Turkish population.

Bilgen T, Tosun O, Luleci G, Keser I. Bilgen T, et al. Among authors: keser i. Genetika. 2008 Aug;44(8):1133-6. Genetika. 2008. PMID: 18825963

6

Premature centromere division in three unrelated families.

Keser I, Lüleci G, Gündüz G. Keser I, et al. Ann Genet. 1996;39(2):87-90. Ann Genet. 1996. PMID: 8766139

7

Molecular analysis of fragile X syndrome in Antalya Province.

Bilgen T, Keser I, Mihci E, Haspolat S, Tacoy S, Luleci G. Bilgen T, et al. Among authors: keser i. Indian J Med Sci. 2005 Apr;59(4):150-5. Indian J Med Sci. 2005. PMID: 15876779

8

The effect of MDR1 (ABCB1) polymorphism on the pharmacokinetic of tacrolimus in Turkish renal transplant recipients.

Akbas SH, Bilgen T, Keser I, Tuncer M, Yucetin L, Tosun O, Gultekin M, Luleci G. Akbas SH, et al. Among authors: keser i. Transplant Proc. 2006 Jun;38(5):1290-2. doi: 10.1016/j.transproceed.2006.02.079. Transplant Proc. 2006. PMID: 16797284

9

Two novel mutations in the 3' untranslated region of the beta-globin gene that are associated with the mild phenotype of beta thalassemia.

Bilgen T, Clark OA, Ozturk Z, Akif Yesilipek M, Keser I. Bilgen T, et al. Among authors: keser i. Int J Lab Hematol. 2013 Feb;35(1):26-30. doi: 10.1111/j.1751-553X.2012.01456.x. Epub 2012 Aug 2. Int J Lab Hematol. 2013. PMID: 22862814

10

Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).

Cetin Z, Mihci E, Keser I, Luleci G. Cetin Z, et al. Among authors: keser i. Genet Couns. 2012;23(2):207-14. Genet Couns. 2012. PMID: 22876579

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

110 results

Search Page

Filters