Nur BG - Search Results

1

Comprehensive dental management in a Hallermann-Streiff syndrome patient with unusual radiographic appearance of teeth.

Gungor OE, Nur BG, Yalcin H, Karayilmaz H, Mihci E. Gungor OE, et al. Among authors: nur bg. Niger J Clin Pract. 2015 Jul-Aug;18(4):559-62. doi: 10.4103/1119-3077.156910. Niger J Clin Pract. 2015. PMID: 25966733

2

Possible autosomal recessive inheritance in an infant with acrofacial dysostosis similar to Nager syndrome.

Nur BG, Bernier FP, Oztekin O, Kardelen F, Kalay S, Parboosingh JS, Mihci E. Nur BG, et al. Am J Med Genet A. 2013 Sep;161A(9):2311-5. doi: 10.1002/ajmg.a.36051. Epub 2013 Aug 2. Am J Med Genet A. 2013. PMID: 23913624

3

Clinical expression of familial Williams-Beuren syndrome in a Turkish family.

Parlak M, Nur BG, Mıhçı E, Durmaz E, Karaüzüm SB, Akcurin S, Bircan İ. Parlak M, et al. Among authors: nur bg. J Pediatr Endocrinol Metab. 2014 Jan;27(1-2):153-8. doi: 10.1515/jpem-2013-0167. J Pediatr Endocrinol Metab. 2014. PMID: 24057591

4

The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation.

Nur BG, Altıok-Clark O, Toylu A, Lüleci G, Mıhçı E. Nur BG, et al. Turk J Pediatr. 2013 Sep-Oct;55(5):559-63. Turk J Pediatr. 2013. PMID: 24382544

5

Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.

Nur BG, Pehlivanoğlu S, Mıhçı E, Calışkan M, Demir D, Alper OM, Kayserili H, Lüleci G. Nur BG, et al. Pediatr Neurol. 2014 May;50(5):482-90. doi: 10.1016/j.pediatrneurol.2014.01.023. Epub 2014 Jan 11. Pediatr Neurol. 2014. PMID: 24656465 Review.

6

Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation.

Nur BG, Gencpinar P, Yuzbasıoglu A, Emre SD, Mihci E. Nur BG, et al. Eur J Med Genet. 2015 Apr;58(4):238-42. doi: 10.1016/j.ejmg.2015.01.011. Epub 2015 Feb 14. Eur J Med Genet. 2015. PMID: 25682902

7

A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type I.

Kilic E, Yigit G, Utine GE, Wollnik B, Mihci E, Nur BG, Boduroglu K. Kilic E, et al. Among authors: nur bg. Am J Med Genet A. 2015 Apr;167A(4):919-21. doi: 10.1002/ajmg.a.36955. Epub 2015 Mar 3. Am J Med Genet A. 2015. PMID: 25735804 No abstract available.

8

Neonatal multiple sulfatase deficiency with a novel mutation and review of the literature.

Nur BG, Mıhçı E, Pepe S, Biberoğlu G, Ezgü FS, Ballabio A, Öztekin O, Dursun O. Nur BG, et al. Turk J Pediatr. 2014 Jul-Aug;56(4):418-22. Turk J Pediatr. 2014. PMID: 25818962 Review.

9

Bilateral congenital cataracts in an infant with Klinefelter syndrome.

Nur BG, Altıok-Clark Ö, İlhan HD, Sayar E, Yücel İ, Mıhçı E. Nur BG, et al. Turk J Pediatr. 2014 Sep-Oct;56(5):546-50. Turk J Pediatr. 2014. PMID: 26022594

10

22q11.2 syndrome due to maternal translocation t(18;22) (pl1.2;q11.2).

Nur BG, Cetin Z, Clark OA, Mihci E, Oygur N, Karauzum SB. Nur BG, et al. Genet Couns. 2015;26(1):67-75. Genet Couns. 2015. PMID: 26043510

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