Hazan 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: hazan 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

Pontocerebellar hypoplasia type III (CLAM): extended phenotype and novel molecular findings.

Durmaz B, Wollnik B, Cogulu O, Li Y, Tekgul H, Hazan F, Ozkinay F. Durmaz B, et al. Among authors: hazan f. J Neurol. 2009 Mar;256(3):416-9. doi: 10.1007/s00415-009-0094-0. Epub 2009 Mar 14. J Neurol. 2009. PMID: 19277761

3

A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family.

Hazan F, Ostergaard P, Ozturk T, Kantekin E, Atlihan F, Jeffery S, Ozkinay F. Hazan F, et al. Am J Med Genet A. 2012 Jul;158A(7):1686-9. doi: 10.1002/ajmg.a.35371. Epub 2012 May 31. Am J Med Genet A. 2012. PMID: 22653704 Free article.

4

A cardio-facio-cutaneous syndrome case with tight Achilles tendons.

Hazan F, Aykut A, Hizarcioglu M, Tavli V, Onay H, Ozkinay F. Hazan F, et al. Genet Couns. 2012;23(2):305-11. Genet Couns. 2012. PMID: 22876591

5

Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3.

Korkmaz HA, Hazan F, Dizdarer C, Tükün A. Korkmaz HA, et al. Among authors: hazan f. J Clin Res Pediatr Endocrinol. 2012 Dec;4(4):220-2. doi: 10.4274/jcrpe.787. Epub 2012 Nov 12. J Clin Res Pediatr Endocrinol. 2012. PMID: 23149434 Free PMC article.

6

A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.

Hazan F, Ozturk AT, Adibelli H, Unal N, Tukun A. Hazan F, et al. Mol Vis. 2013;19:196-202. Epub 2013 Jan 29. Mol Vis. 2013. PMID: 23378733 Free PMC article.

7

Ventricular septal defect in Crouzon Syndrome: case report.

Hazan F, Aykut A, Unalp A, Mese T, Unal N, Onay H, Ozkinay F. Hazan F, et al. Genet Couns. 2012;23(4):519-22. Genet Couns. 2012. PMID: 23431754 No abstract available.

8

A novel mutation, IVS13+5G>A, in Ellis-van Creveld syndrome associated with haemophagocytic lymphohistiocytosis.

Zeytinoglu M, Aykut A, Hazan F, Torrente I, Akay MC, Karapinar DY, Vergin C, Cogulu O, Ozkinay F. Zeytinoglu M, et al. Among authors: hazan f. Clin Dysmorphol. 2013 Oct;22(4):140-142. doi: 10.1097/MCD.0b013e3283633831. Clin Dysmorphol. 2013. PMID: 23924873 No abstract available.

9

Histopathological and genetic features of patients with limb girdle muscular dystrophy type 2C.

Dınız G, Hazan F, Yildirim HT, Unalp A, Polat M, Serdaroğlu G, Güzel O, Bağ O, Seçıl Y, Ozgönül F, Türe S, Akhan G, Tükün A. Dınız G, et al. Among authors: hazan f. Turk Patoloji Derg. 2014;30(2):111-7. doi: 10.5146/tjpath.2014.01239. Turk Patoloji Derg. 2014. PMID: 24638197 Free article.

10

Sarcolemmal alpha and gamma sarcoglycan protein deficiencies in Turkish siblings with a novel missense mutation in the alpha sarcoglycan gene.

Diniz G, Tosun Yildirim H, Akinci G, Hazan F, Ozturk A, Yararbas K, Tukun A. Diniz G, et al. Among authors: hazan f. Pediatr Neurol. 2014 Jun;50(6):640-7. doi: 10.1016/j.pediatrneurol.2013.12.024. Epub 2014 Jan 25. Pediatr Neurol. 2014. PMID: 24742800

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

60 results

Search Page

Filters