Ozkinay F - Search Results

1

A novel mutation in two families with pycnodysostosis.

Ozdemir TR, Atik T, Karaca E, Onay H, Ozkinay F, Cogulu O. Ozdemir TR, et al. Among authors: ozkinay f. Clin Dysmorphol. 2013 Jul;22(3):102-105. doi: 10.1097/MCD.0b013e3283619632. Clin Dysmorphol. 2013. PMID: 23689398 No abstract available.

2

New chromosome rearrangement in acute lymphoblastic leukemia.

Gündüz C, Coğulu O, Cetingül N, Kantar M, Cankaya T, Ozkinay C, Ozkinay F. Gündüz C, et al. Among authors: ozkinay f, ozkinay c. Cancer Genet Cytogenet. 2002 Sep;137(2):150-2. doi: 10.1016/s0165-4608(02)00561-7. Cancer Genet Cytogenet. 2002. PMID: 12393288

3

Highest heterogeneity for cystic fibrosis: 36 mutations account for 75% of all CF chromosomes in Turkish patients.

Kilinç MO, Ninis VN, Dağli E, Demirkol M, Ozkinay F, Arikan Z, Coğulu O, Hüner G, Karakoç F, Tolun A. Kilinç MO, et al. Among authors: ozkinay f. Am J Med Genet. 2002 Dec 1;113(3):250-7. doi: 10.1002/ajmg.10721. Am J Med Genet. 2002. PMID: 12439892

4

Valproic acid and lamotrigine treatment during pregnancy. The risk of chromosomal abnormality.

Ozkinay F, Cogulu O, Gunduz C, Yilmaz D, Kultursay N. Ozkinay F, et al. Mutat Res. 2003 Jan 10;534(1-2):197-9. doi: 10.1016/s1383-5718(02)00254-1. Mutat Res. 2003. PMID: 12504768

5

Sliding type hernia and ectopic pancreatic tissue in the stomach with renal agenesis and ear abnormalities: branchio-oto-renal syndrome or hemifacial microsomia with additional findings.

Ozkinay F, Cogulu O, Ozkinay C, Aydogdu S, Gunduz C, Tacoy S. Ozkinay F, et al. Among authors: ozkinay c. Am J Med Genet A. 2003 Aug 1;120A(4):562-3. doi: 10.1002/ajmg.a.20109. Am J Med Genet A. 2003. PMID: 12884440 No abstract available.

6

Celiac disease in children with Down syndrome: importance of follow-up and serologic screening.

Cogulu O, Ozkinay F, Gunduz C, Cankaya T, Aydogdu S, Ozgenc F, Kutukculer N, Ozkinay C. Cogulu O, et al. Among authors: ozkinay f, ozkinay c. Pediatr Int. 2003 Aug;45(4):395-9. doi: 10.1046/j.1442-200x.2003.01755.x. Pediatr Int. 2003. PMID: 12911473

7

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

8

Evaluation of 80 children with prolonged fever.

Cogulu O, Koturoglu G, Kurugol Z, Ozkinay F, Vardar F, Ozkinay C. Cogulu O, et al. Among authors: ozkinay f, ozkinay c. Pediatr Int. 2003 Oct;45(5):564-9. doi: 10.1046/j.1442-200x.2003.01793.x. Pediatr Int. 2003. PMID: 14521533

9

Hair zinc level in Down syndrome.

Yenigun A, Ozkinay F, Cogulu O, Coker C, Cetiner N, Ozden G, Aksu O, Ozkinay C. Yenigun A, et al. Among authors: ozkinay f, ozkinay c. Downs Syndr Res Pract. 2004 Jul;9(2):53-7. doi: 10.3104/reports.292. Downs Syndr Res Pract. 2004. PMID: 15332439 Free article.

10

Evaluation of telomerase mRNA (hTERT) in childhood acute leukemia.

Cogulu O, Kosova B, Karaca E, Gunduz C, Ozkinay F, Aksoylar S, Gulen H, Kantar M, Oniz H, Karapinar D, Cetingul N, Erbay A, Vergin C, Ozkinay C. Cogulu O, et al. Among authors: ozkinay f, ozkinay c. Leuk Lymphoma. 2004 Dec;45(12):2477-80. doi: 10.1080/10428190400007508. Leuk Lymphoma. 2004. PMID: 15621763

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