Onay H - Search Results

1

Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations.

Aykut A, Karaca E, Onay H, Gökşen D, Çetinkalp Ş, Eren E, Ersoy B, Çakır EP, Büyükinan M, Kara C, Anık A, Kırel B, Özen S, Atik T, Darcan Ş, Özkınay F. Aykut A, et al. Among authors: onay h. Gene. 2018 Jan 30;641:186-189. doi: 10.1016/j.gene.2017.10.057. Epub 2017 Oct 19. Gene. 2018. PMID: 29056535

2

Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: a comparative study for four years.

Gunduz C, Cogulu O, Cankaya T, Bora E, Karaca E, Alpman A, Sagol S, Onay H, Ozkinay F, Ozkinay C. Gunduz C, et al. Among authors: onay h. Genet Couns. 2004;15(1):53-9. Genet Couns. 2004. PMID: 15083700

3

Two extra euchromatic bands in the qh region of chromosome 9.

Ozkinay F, Ercal D, Ozkinay C, Onay H, Bora E, Erler A. Ozkinay F, et al. Among authors: onay h. Genet Couns. 2005;16(1):45-8. Genet Couns. 2005. PMID: 15844778

4

Exon-3 polymorphism of CTLA-4 gene in Turkish patients with vitiligo.

Itirli G, Pehlivan M, Alper S, Yüksel SE, Onay H, Ozkinay F, Pehlivan S. Itirli G, et al. Among authors: onay h. J Dermatol Sci. 2005 Jun;38(3):225-7. doi: 10.1016/j.jdermsci.2005.03.003. J Dermatol Sci. 2005. PMID: 15888380 No abstract available.

5

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: onay h. Clin Dysmorphol. 2005 Jul;14(3):161-164. Clin Dysmorphol. 2005. PMID: 15930910

6

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: onay h. 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.

7

Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.

Ozkinay F, Kanit H, Onay H, Cogulu O, Gunduz C, Ercal D, Ozkinay C. Ozkinay F, et al. Among authors: onay h. Genet Couns. 2006;17(3):315-20. Genet Couns. 2006. PMID: 17100200

8

Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization.

Cogulu O, Gunduz C, Karaca E, Onay H, Ozkinay C, Ozkinay F. Cogulu O, et al. Among authors: onay h. Genet Couns. 2006;17(3):321-31. Genet Couns. 2006. PMID: 17100201

9

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. 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

10

Duane anomaly, meningomyelocele, dextroposition of heart and localized vertebrocostal alterations with associated anomalies in a girl.

Cogulu O, Gunduz C, Karaca E, Onay H, Superti-Furga A, Ozkinay F. Cogulu O, et al. Among authors: onay h. Genet Couns. 2007;18(1):77-83. Genet Couns. 2007. PMID: 17515303

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