Boduroğlu K - Search Results

1

Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 gene.

Kiliç E, Alanay Y, Utine E, Ozgen-Mocan B, Robinson PN, Boduroğlu K. Kiliç E, et al. Among authors: boduroglu k. Turk J Pediatr. 2012 Mar-Apr;54(2):198-202. Turk J Pediatr. 2012. PMID: 22734312

2

Results of the Turkish congenital malformation survey.

Tunçbilek E, Boduroğlu K, Alikaşifoğlu M. Tunçbilek E, et al. Among authors: boduroglu k. Turk J Pediatr. 1999 Jul-Sep;41(3):287-97. Turk J Pediatr. 1999. PMID: 10770088

3

Neural tube defects in Turkey: prevalence, distribution and risk factors.

Tunçbilek E, Boduroğlu K, Alikaşifoğlu M. Tunçbilek E, et al. Among authors: boduroglu k. Turk J Pediatr. 1999 Jul-Sep;41(3):299-305. Turk J Pediatr. 1999. PMID: 10770089

4

A Turkish family with Greig cephalopolysyndactyly syndrome.

Boduroğlu K, Balci S, Topçu M. Boduroğlu K, et al. Turk J Pediatr. 1999 Apr-Jun;41(2):259-65. Turk J Pediatr. 1999. PMID: 10770668

5

Two siblings with Bloom's syndrome exhibit different clinical features: possible effect of sex.

Boduroğlu K, Tunçbilek E. Boduroğlu K, et al. Turk J Pediatr. 1999 Jan-Mar;41(1):107-11. Turk J Pediatr. 1999. PMID: 10770684

6

Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly.

Balci S, Boduroğlu K, Kaya S. Balci S, et al. Among authors: boduroglu k. Turk J Pediatr. 2001 Oct-Dec;43(4):362-5. Turk J Pediatr. 2001. PMID: 11765172

7

Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for Down syndrome among Turkish women.

Boduroğlu K, Alanay Y, Koldan B, Tunçbilek E. Boduroğlu K, et al. Am J Med Genet A. 2004 May 15;127A(1):5-10. doi: 10.1002/ajmg.a.20432. Am J Med Genet A. 2004. PMID: 15103709

8

Oculo-palato-cerebral syndrome: a third case supporting autosomal recessive inheritance.

Alanay Y, Boduroglu K, Sönmez B, Orhan M. Alanay Y, et al. Among authors: boduroglu k. Am J Med Genet A. 2004 Sep 15;130A(1):92-5. doi: 10.1002/ajmg.a.30114. Am J Med Genet A. 2004. PMID: 15368502

9

Celiac disease screening in 100 Turkish children with Down syndrome.

Alanay Y, Boduroğlu K, Tunçbilek E. Alanay Y, et al. Among authors: boduroglu k. Turk J Pediatr. 2005 Apr-Jun;47(2):138-40. Turk J Pediatr. 2005. PMID: 16052853

10

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. Turk J Pediatr. 2005 Oct-Dec;47(4):327-33. Turk J Pediatr. 2005. PMID: 16363341

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