Alanay Y - Search Results

1

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

2

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. Among authors: alanay y. 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

3

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

Alanay Y, Boduroglu K, Sönmez B, Orhan M. Alanay Y, et al. 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

4

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. 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.

5

Celiac disease screening in 100 Turkish children with Down syndrome.

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

6

Spondylo-ocular syndrome: a new entity involving the eye and spine.

Alanay Y, Superti-Furga A, Karel F, Tunçbilek E. Alanay Y, et al. Am J Med Genet A. 2006 Mar 15;140(6):652-6. doi: 10.1002/ajmg.a.31119. Am J Med Genet A. 2006. PMID: 16470687 No abstract available.

7

Terminal phalangeal accessory ossification center of the thumb: an additional radiographic finding in Larsen syndrome.

Alanay Y, Utine GE, Lachman RS, Krakow D, Tuncbilek E. Alanay Y, et al. Pediatr Radiol. 2006 Sep;36(9):970-3. doi: 10.1007/s00247-006-0217-z. Epub 2006 May 20. Pediatr Radiol. 2006. PMID: 16715218

8

Congenital contractural arachnodactyly (Beals syndrome).

Tunçbilek E, Alanay Y. Tunçbilek E, et al. Among authors: alanay y. Orphanet J Rare Dis. 2006 Jun 1;1:20. doi: 10.1186/1750-1172-1-20. Orphanet J Rare Dis. 2006. PMID: 16740166 Free PMC article. Review.

9

A multidisciplinary approach to the management of individuals with fragile X syndrome.

Alanay Y, Unal F, Turanli G, Alikaşifoğlu M, Alehan D, Akyol U, Belgin E, Sener C, Aktaş D, Boduroğlu K, Utine E, Volkan-Salanci B, Ozusta S, Genç A, Başar F, Sevinç S, Tunçbilek E. Alanay Y, et al. J Intellect Disabil Res. 2007 Feb;51(Pt 2):151-61. doi: 10.1111/j.1365-2788.2006.00942.x. J Intellect Disabil Res. 2007. PMID: 17217479

10

Cerebro-facio-thoracic dysplasia: expanding the phenotype.

Cilliers D, Alanay Y, Boduroglu K, Utine E, Tunçbilek E, Clayton-Smith J. Cilliers D, et al. Among authors: alanay y. Clin Dysmorphol. 2007 Apr;16(2):121-125. doi: 10.1097/MCD.0b013e328012e292. Clin Dysmorphol. 2007. PMID: 17351359

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