Aktaş D - Search Results

1

A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype.

Simşek-Kiper PO, Utine GE, Alanay Y, Aktaş D, Alikaşifoğlu M, Boduroğlu K. Simşek-Kiper PO, et al. Among authors: aktas d. Turk J Pediatr. 2011 Sep-Oct;53(5):558-60. Turk J Pediatr. 2011. PMID: 22272459

2

Diploid-triploid and tetraploid mosaicism in a child with cryptogenic cirrhosis and membranous glomerulonephritis: a causal relationship or coincidental association?

Topaloğlu R, Aktaş D, Bakkaloğlu A, Balci S, Doğru D, Oztürk R. Topaloğlu R, et al. Among authors: aktas d. Turk J Pediatr. 1998 Jan-Mar;40(1):139-43. Turk J Pediatr. 1998. PMID: 9673542

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

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

5

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

6

CYP1A1 gene polymorphism and risk of epithelial ovarian neoplasm.

Aktas D, Guney I, Alikasifoglu M, Yüce K, Tuncbilek E, Ayhan A. Aktas D, et al. Gynecol Oncol. 2002 Aug;86(2):124-8. doi: 10.1006/gyno.2002.6720. Gynecol Oncol. 2002. PMID: 12144816

7

Is Dandy-Walker malformation associated with "distal 13q deletion syndrome"? Findings in a fetus supporting previous observations.

Alanay Y, Aktaş D, Utine E, Talim B, Onderoğlu L, Cağlar M, Tunçbilek E. Alanay Y, et al. Among authors: aktas d. Am J Med Genet A. 2005 Jul 30;136(3):265-8. doi: 10.1002/ajmg.a.30808. Am J Med Genet A. 2005. PMID: 15948192 Review.

8

Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.

Boduroğlu K, Alanay Y, Alikaşifoğlu M, Aktaş D, Tunçbilek E. Boduroğlu K, et al. Among authors: aktas d. Turk J Pediatr. 2005 Oct-Dec;47(4):327-33. Turk J Pediatr. 2005. PMID: 16363341

9

CYP1A1 gene polymorphism as a risk factor for cervical intraepithelial neoplasia and invasive cervical cancer.

Taskiran C, Aktas D, Yigit-Celik N, Alikasifoglu M, Yuce K, Tunçbilek E, Ayhan A. Taskiran C, et al. Among authors: aktas d. Gynecol Oncol. 2006 Jun;101(3):503-6. doi: 10.1016/j.ygyno.2005.11.018. Epub 2006 Jan 5. Gynecol Oncol. 2006. PMID: 16403567

10

Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.

Aktas D, Alikasifoglu M, Gonc N, Senocak ME, Tuncbilek E. Aktas D, et al. Eur J Med Genet. 2006 Mar-Apr;49(2):141-9. doi: 10.1016/j.ejmg.2005.05.012. Epub 2005 Jul 1. Eur J Med Genet. 2006. PMID: 16530711

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