Sag SO - Search Results

1

Genotype and Phenotype Correlation of Patients with Osteogenesis Imperfecta.

Aliyeva L, Ongen YD, Eren E, Sarisozen MB, Alemdar A, Temel SG, Sag SO. Aliyeva L, et al. Among authors: sag so. J Mol Diagn. 2024 Sep;26(9):754-769. doi: 10.1016/j.jmoldx.2024.05.014. Epub 2024 Jul 20. J Mol Diagn. 2024. PMID: 39025364

2

A NOVEL MUTATION IN NPR2 GENE IN A PATIENT WITH ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE.

Sag SO, Gorukmez O, Topak A, Gorukmez O, Ture M, Sahinturk S, Gulten T, Yakut T. Sag SO, et al. Genet Couns. 2015;26(2):219-25. Genet Couns. 2015. PMID: 26349192

3

NOVEL MUTATION OF THE ELECTRON TRANSFERRING FLAVOPROTEIN DEHYDROGENASE (ETFDH) GENE IN THE ISOLATED MYOPATHIC FORM OF COENZYME q10 DEFICIENCY.

Gorukmez O, Gorukmez O, Sag SO, Erdol S, Saglam H, Yakut T. Gorukmez O, et al. Among authors: sag so. Genet Couns. 2015;26(2):259-62. Genet Couns. 2015. PMID: 26349199 No abstract available.

4

TURNER SYNDROME WITH 45,X/46,X,I(Xq)/47,X,I(Xq),I(Xq) KARYOTYPE.

Gorukmez O, Sag SO, Gulten T, Gorukmez, Ture M, Yakut T. Gorukmez O, et al. Among authors: sag so. Genet Couns. 2015;26(2):267-9. Genet Couns. 2015. PMID: 26349201 No abstract available.

5

De novo partial trisomy distal 4q: a case report.

Gorukmez O, Sag SO, Gorukmez O, Ture M, Gulten T, Yakut T. Gorukmez O, et al. Among authors: sag so. Genet Couns. 2014;25(4):423-8. Genet Couns. 2014. PMID: 25804022

6

Associations analysis of GSTM1, T1 and P1 Ile105Val polymorphisms with carpal tunnel syndrome.

Eroğlu P, Erkol İnal E, Sağ ŞÖ, Görükmez Ö, Topak A, Yakut T. Eroğlu P, et al. Among authors: sag so. Clin Rheumatol. 2016 May;35(5):1245-51. doi: 10.1007/s10067-014-2855-0. Epub 2015 Jan 9. Clin Rheumatol. 2016. PMID: 25566970

7

MICROARRAY DELINEATION OF DE NOVO DUPLICATION 1q32q42 IN A CHILD SHOWING MULTIPLE ANOMALIES AND DYSMORPHISM.

Gorukmez O, Aydin H, Gorukmez O, Sag SO, Kucukcongar A, Celayir FM. Gorukmez O, et al. Among authors: sag so. Genet Couns. 2015;26(2):181-6. Genet Couns. 2015. PMID: 26349187

8

Characterization and in silico analyses of the BRCA1/2 variants identified in individuals with personal and/or family history of BRCA-related cancers.

Pirim D, Kaya N, Yıldırım EU, Sag SO, Temel SG. Pirim D, et al. Among authors: sag so. Int J Biol Macromol. 2020 Nov 1;162:1166-1177. doi: 10.1016/j.ijbiomac.2020.06.222. Epub 2020 Jun 26. Int J Biol Macromol. 2020. PMID: 32599251

9

Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia.

Tuncel G, Akcan N, Gul S, Sag SO, Bundak R, Mocan G, Temel SG, Ergoren MC. Tuncel G, et al. Among authors: sag so. Appl Immunohistochem Mol Morphol. 2021 Aug 1;29(7):546-550. doi: 10.1097/PAI.0000000000000914. Appl Immunohistochem Mol Morphol. 2021. PMID: 33595934

10

Inconsistency of Karyotyping and Array Comparative Genomic Hybridization (aCGH) in a Mosaic Turner Syndrome Case.

Tulay P, Ergoren MC, Alkaya A, Yayci E, Sag SO, Temel SG. Tulay P, et al. Among authors: sag so. Glob Med Genet. 2020 Dec;7(4):128-132. doi: 10.1055/s-0041-1722974. Epub 2021 Feb 11. Glob Med Genet. 2020. PMID: 33693446 Free PMC article.

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

29 results

Search Page

Filters