Demirhan O - Search Results

1

Barttin mutations in antenatal Bartter syndrome with sensorineural deafness.

Ozlu F, Yapicioğlu H, Satar M, Narli N, Ozcan K, Buyukcelik M, Konrad M, Demirhan O. Ozlu F, et al. Among authors: demirhan o. Pediatr Nephrol. 2006 Jul;21(7):1056-7. doi: 10.1007/s00467-006-0108-4. Epub 2006 May 24. Pediatr Nephrol. 2006. PMID: 16773427 Free article. No abstract available.

2

A case of spondylocostal dysostosis with a fra (5) (q32).

Satar M, Temoçin AK, Atici A, Demirhan O. Satar M, et al. Among authors: demirhan o. Turk J Pediatr. 1997 Oct-Dec;39(4):547-9. Turk J Pediatr. 1997. PMID: 9433158

3

Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine sampling.

Demirhan O, Ozcan K, Taştemir D, Demir C, Tunç E, Solğun HA, Güzel AI. Demirhan O, et al. Fertil Steril. 2008 Jan;89(1):228.e1-6. doi: 10.1016/j.fertnstert.2007.02.030. Epub 2007 Sep 19. Fertil Steril. 2008. PMID: 17880960 Free article.

4

Cytogenetic effects of ethanol on chronic alcohol users.

Demirhan O, Tastemir D. Demirhan O, et al. Alcohol Alcohol. 2008 Mar-Apr;43(2):127-36. doi: 10.1093/alcalc/agm155. Epub 2008 Jan 18. Alcohol Alcohol. 2008. PMID: 18204049

5

Phenotypic correlations in a patient with ring chromosome 22.

Demirhan O, Tunç E. Demirhan O, et al. Indian J Hum Genet. 2010 May;16(2):97-9. doi: 10.4103/0971-6866.69372. Indian J Hum Genet. 2010. PMID: 21031059 Free PMC article.

6

Polymorphisms in NRAMP1 and MBL2 genes and their relations with tuberculosis in Turkish children.

Solğun HA, Taştemir D, Aksaray N, Inan I, Demirhan O. Solğun HA, et al. Among authors: demirhan o. Tuberk Toraks. 2011;59(1):48-53. doi: 10.5578/tt.2385. Tuberk Toraks. 2011. PMID: 21554230 Free article.

7

Chromosomal analyses of 1510 couples who have experienced recurrent spontaneous abortions.

Tunç E, Tanrıverdi N, Demirhan O, Süleymanova D, Çetinel N. Tunç E, et al. Among authors: demirhan o. Reprod Biomed Online. 2016 Apr;32(4):414-9. doi: 10.1016/j.rbmo.2016.01.006. Epub 2016 Jan 28. Reprod Biomed Online. 2016. PMID: 26874988

8

Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients.

Demirhan O, Tunç E. Demirhan O, et al. Chromosoma. 2022 Dec;131(4):225-237. doi: 10.1007/s00412-022-00782-3. Epub 2022 Oct 11. Chromosoma. 2022. PMID: 36219240

9

Cytogenetic study of recurrent miscarriages and their parents.

Tunç E, Demirhan O, Demir C, Tastemir D. Tunç E, et al. Among authors: demirhan o. Genetika. 2007 Apr;43(4):545-52. Genetika. 2007. PMID: 17555132 Clinical Trial.

10

Alterations in p16 and p53 genes and chromosomal findings in patients with lung cancer: fluorescence in situ hybridization and cytogenetic studies.

Demirhan O, Taştemir D, Hastürk S, Kuleci S, Hanta I. Demirhan O, et al. Cancer Epidemiol. 2010 Aug;34(4):472-7. doi: 10.1016/j.canep.2010.03.018. Epub 2010 May 4. Cancer Epidemiol. 2010. PMID: 20444664

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