Ozkinay F - Search Results

1

Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations.

Atik T, Aykut A, Hazan F, Onay H, Goksen D, Darcan S, Tukun A, Ozkinay F. Atik T, et al. Among authors: ozkinay f. Indian J Pediatr. 2016 Jun;83(6):517-21. doi: 10.1007/s12098-015-1998-6. Epub 2016 Jan 28. Indian J Pediatr. 2016. PMID: 26817465

2

Multiple pterygium syndrome.

Ozkinay FF, Ozkinay C, Akin H, Azarsiz S, Gündüz C. Ozkinay FF, et al. Among authors: ozkinay c. Indian J Pediatr. 1997 Jan-Feb;64(1):113-6. doi: 10.1007/BF02795791. Indian J Pediatr. 1997. PMID: 10771823

3

Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene.

Pehlivan S, Ozkinay F, Okutman O, Coğulu O, Ozcan A, Cankaya T, Ulgenalp A. Pehlivan S, et al. Among authors: ozkinay f. Turk J Pediatr. 2003 Apr-Jun;45(2):99-101. Turk J Pediatr. 2003. PMID: 12921294

4

Trigonocephaly and Wilson's disease in two siblings.

Cogulu O, Onay H, Ozgenc F, Karaca E, Gunduz C, Tzetis M, Cankaya T, Kanavakis E, Ozkinay F. Cogulu O, et al. Among authors: ozkinay f. Clin Dysmorphol. 2005 Jul;14(3):161-164. Clin Dysmorphol. 2005. PMID: 15930910

5

A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia.

Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK. Garg A, et al. Among authors: ozkinay f. J Clin Endocrinol Metab. 2005 Sep;90(9):5259-64. doi: 10.1210/jc.2004-2560. Epub 2005 Jul 5. J Clin Endocrinol Metab. 2005. PMID: 15998779 Review.

6

Might there be a link between mannose binding lectin and vitiligo?

Onay H, Pehlivan M, Alper S, Ozkinay F, Pehlivan S. Onay H, et al. Among authors: ozkinay f. Eur J Dermatol. 2007 Mar-Apr;17(2):146-8. doi: 10.1684/ejd.2007.0128. Epub 2007 Mar 2. Eur J Dermatol. 2007. PMID: 17337399

7

Two cases of macrocephaly and immune deficiency.

Cogulu O, Aykut A, Kutukculer N, Ozkinay C, Ozkinay F. Cogulu O, et al. Among authors: ozkinay f, ozkinay c. Clin Dysmorphol. 2007 Apr;16(2):81-84. doi: 10.1097/MCD.0b013e3280464ee6. Clin Dysmorphol. 2007. PMID: 17351349

8

Evidence of an association between mannose binding lectin codon 54 polymorphism and adenoidectomy and/or tonsillectomy in children.

Koturoglu G, Onay H, Midilli R, Pehlivan S, Eren E, Itirli G, Kurugol Z, Apaydin F, Ozkinay C, Ozkinay F. Koturoglu G, et al. Among authors: ozkinay f, ozkinay c. Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1157-61. doi: 10.1016/j.ijporl.2007.05.004. Epub 2007 Jun 7. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17559949

9

Purine nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections.

Ozkinay F, Pehlivan S, Onay H, van den Berg P, Vardar F, Koturoglu G, Aksu G, Unal D, Tekgul H, Can S, Ozkinay C. Ozkinay F, et al. Among authors: ozkinay c. J Child Neurol. 2007 Jun;22(6):741-3. doi: 10.1177/0883073807302617. J Child Neurol. 2007. PMID: 17641261

10

Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis.

Vardar F, Pehlivan S, Onay H, Atlihan F, Güliz N, Ozkinay C, Ozkinay F. Vardar F, et al. Among authors: ozkinay f, ozkinay c. Turk J Pediatr. 2007 Jul-Sep;49(3):270-3. Turk J Pediatr. 2007. PMID: 17990579

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

305 results

Search Page

Filters