Toksoy G - Search Results

1

The results of cytogenetic analysis with regard to intracytoplasmic sperm injection in males, females and fetuses.

Basaran S, Engur A, Aytan M, Karaman B, Ghanbari A, Toksoy G, Yuksel A, Cankat D, Kervancioglu E, Wollnik B, Bahceci M, Yuksel-Apak M. Basaran S, et al. Among authors: toksoy g. Fetal Diagn Ther. 2004 Jul-Aug;19(4):313-8. doi: 10.1159/000077958. Fetal Diagn Ther. 2004. PMID: 15192289

2

The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.

Karaman B, Aytan M, Yilmaz K, Toksoy G, Onal EP, Ghanbari A, Engur A, Kayserili H, Yuksel-Apak M, Basaran S. Karaman B, et al. Among authors: toksoy g. Eur J Med Genet. 2006 May-Jun;49(3):207-14. doi: 10.1016/j.ejmg.2005.06.002. Epub 2005 Jul 12. Eur J Med Genet. 2006. PMID: 16762822

3

Mutational screening of BASP1 and transcribed processed pseudogene TPPsig-BASP1 in patients with Möbius syndrome.

Uzumcu A, Candan S, Toksoy G, Uyguner ZO, Karaman B, Eris H, Tatli B, Kayserili H, Yuksel A, Geckinli B, Yuksel-Apak M, Basaran S. Uzumcu A, et al. Among authors: toksoy g. J Genet Genomics. 2009 Apr;36(4):251-6. doi: 10.1016/S1673-8527(08)60112-5. J Genet Genomics. 2009. PMID: 19376485

4

Molecular genetic screening of MBS1 locus on chromosome 13 for microdeletions and exclusion of FGF9, GSH1 and CDX2 as causative genes in patients with Moebius syndrome.

Uzumcu A, Karaman B, Toksoy G, Uyguner ZO, Candan S, Eris H, Tatli B, Geckinli B, Yuksel A, Kayserili H, Basaran S. Uzumcu A, et al. Among authors: toksoy g. Eur J Med Genet. 2009 Sep-Oct;52(5):315-20. doi: 10.1016/j.ejmg.2009.05.003. Epub 2009 May 19. Eur J Med Genet. 2009. PMID: 19460469

5

Left diaphragmatic eventration associated with ipsilateral pulmonary sequestration and intrathoracic kidney in a fetus: reviewing the prenatal diagnosis and etiopathogenesis.

Sahinoglu Z, Yuksel A, Uludogan M, Bilgic R, Toksoy G. Sahinoglu Z, et al. Among authors: toksoy g. Fetal Pediatr Pathol. 2011;30(4):233-43. doi: 10.3109/15513815.2011.555808. Epub 2011 Mar 24. Fetal Pediatr Pathol. 2011. PMID: 21434828

6

Novel indel Mutation in the GDF5 Gene Is Associated with Brachydactyly Type C in a Four-Generation Turkish Family.

Uyguner ZO, Kocaoğlu M, Toksoy G, Basaran S, Kayserili H. Uyguner ZO, et al. Among authors: toksoy g. Mol Syndromol. 2014 Feb;5(2):81-6. doi: 10.1159/000357264. Epub 2014 Jan 3. Mol Syndromol. 2014. PMID: 24715855 Free PMC article.

7

A new hereditary congenital facial palsy case supports arg5 in HOX-DNA binding domain as possible hot spot for mutations.

Uyguner ZO, Toksoy G, Altunoglu U, Ozgur H, Basaran S, Kayserili H. Uyguner ZO, et al. Among authors: toksoy g. Eur J Med Genet. 2015 Jun-Jul;58(6-7):358-63. doi: 10.1016/j.ejmg.2015.05.003. Epub 2015 May 23. Eur J Med Genet. 2015. PMID: 26007620

8

Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene.

Baş F, Toksoy G, Ergun-Longmire B, Uyguner ZO, Abalı ZY, Poyrazoğlu Ş, Karaman V, Avcı Ş, Altunoğlu U, Bundak R, Karaman B, Başaran S, Darendeliler F. Baş F, et al. Among authors: toksoy g. J Steroid Biochem Mol Biol. 2018 Jul;181:88-97. doi: 10.1016/j.jsbmb.2018.04.001. Epub 2018 Apr 4. J Steroid Biochem Mol Biol. 2018. PMID: 29626607

9

Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.

Karaman B, Kayserili H, Ghanbari A, Uyguner ZO, Toksoy G, Altunoglu U, Basaran S. Karaman B, et al. Among authors: toksoy g. Mol Cytogenet. 2018 Aug 17;11:45. doi: 10.1186/s13039-018-0395-z. eCollection 2018. Mol Cytogenet. 2018. PMID: 30140312 Free PMC article.

10

Clinical and Genetic Investigation of Premature Ovarian Insufficiency Cases from Turkey.

Oral E, Toksoy G, Sofiyeva N, Celik HG, Karaman B, Basaran S, Azami A, Uyguner ZO. Oral E, et al. Among authors: toksoy g. J Gynecol Obstet Hum Reprod. 2019 Dec;48(10):817-823. doi: 10.1016/j.jogoh.2019.04.007. Epub 2019 Apr 23. J Gynecol Obstet Hum Reprod. 2019. PMID: 31026518

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