Aktas D - Search Results

1

Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH.

Utine EG, Alanay Y, Aktas D, Alikasifoglu M, Boduroglu K, Vermeesch J, Tuncbilek E, Fryns JP. Utine EG, et al. Among authors: aktas d. Eur J Med Genet. 2008 Jul-Aug;51(4):343-50. doi: 10.1016/j.ejmg.2008.03.002. Epub 2008 Mar 27. Eur J Med Genet. 2008. PMID: 18440888

2

No evidence for overexpression of the p53 protein and mutations in exons 4-9 of the p53 gene in a large family with adenomatous polyposis.

Aktas D, Ayhan A, Tunçbilek E, Ozdemir A, Uzunalimoğlu B. Aktas D, et al. Am J Gastroenterol. 1998 Sep;93(9):1524-6. doi: 10.1111/j.1572-0241.1998.00414.x. Am J Gastroenterol. 1998. PMID: 9732936

3

Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology.

Tunçbilek E, Alikasifoğlu M, Boduroğlu K, Aktas D, Anar B. Tunçbilek E, et al. Among authors: aktas d. Am J Med Genet. 1999 May 28;84(3):202-3. doi: 10.1002/(sici)1096-8628(19990528)84:3<202::aid-ajmg6>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10331591 No abstract available.

4

Loss of maternal allele in a child with myelodysplastic syndrome and monosomy 7.

Aktas D, Yenicesu I, Hicsonmez G, Tuncbilek E. Aktas D, et al. Am J Hematol. 1999 Sep;62(1):49-51. doi: 10.1002/(sici)1096-8652(199909)62:1<49::aid-ajh8>3.0.co;2-y. Am J Hematol. 1999. PMID: 10467276 Free article.

5

Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient.

Koç A, Oner R, Oner C, Aktas D, Sözen M, Tunçbilek E, Altay C. Koç A, et al. Among authors: aktas d. Hematol Cell Ther. 1999 Aug;41(4):187-9. doi: 10.1007/s00282-999-0187-3. Hematol Cell Ther. 1999. PMID: 10543376

6

Myelodysplastic syndrome associated with monosomy 7 in a child with Bloom syndrome.

Aktas D, Koc A, Boduroglu K, Hicsonmez G, Tuncbilek E. Aktas D, et al. Cancer Genet Cytogenet. 2000 Jan 1;116(1):44-6. doi: 10.1016/s0165-4608(99)00099-0. Cancer Genet Cytogenet. 2000. PMID: 10616531

7

Screening for the fragile X syndrome among mentally retarded males by hair root analysis.

Tunçbilek E, Alikasifoğlu M, Aktas D, Duman F, Yanik H, Anar B, Oostra B, Willemsen R. Tunçbilek E, et al. Among authors: aktas d. Am J Med Genet. 2000 Nov 13;95(2):105-7. doi: 10.1002/1096-8628(20001113)95:2<105::aid-ajmg3>3.0.co;2-6. Am J Med Genet. 2000. PMID: 11078558

8

Glutathione S-transferase M1 gene polymorphism in bladder cancer patients. a marker for invasive bladder cancer?

Aktas D, Ozen H, Atsu N, Tekin A, Sozen S, Tuncbilek E. Aktas D, et al. Cancer Genet Cytogenet. 2001 Feb;125(1):1-4. doi: 10.1016/s0165-4608(00)00307-1. Cancer Genet Cytogenet. 2001. PMID: 11297759

9

Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia. a case report and review of the literature.

Aktas D, Tuncbilek E, Cetin M, Hicsonmez G. Aktas D, et al. Cancer Genet Cytogenet. 2001 Apr 15;126(2):166-8. doi: 10.1016/s0165-4608(00)00403-9. Cancer Genet Cytogenet. 2001. PMID: 11376811 Review.

10

Chromosomal mosaicism in a pregnant woman treated with acyclovir for herpes simplex encephalitis.

Aktas D, Tuncbilek E, Onderoglu L. Aktas D, et al. Am J Perinatol. 2001 Jun;18(4):179-83. doi: 10.1055/s-2001-15501. Am J Perinatol. 2001. PMID: 11444361

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