Publications by authors named "Erdal Tunc"

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A Cytogenetic Study of Turkish Children with Global Developmental Delay.
Osman Demirhan, Özlem Hergüner, Erdal Tunç

J Pediatr Genet· June 2024

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

Chromosoma· December 2022

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Robertsonian translocation (13;14) and its clinical manifestations: a literature review.
Erdal Tunç, Seda Ilgaz

Reprod Biomed Online· September 2022

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Effects of high-molecular-weight polyvinyl chloride on Xenopus laevis adults and embryos: the mRNA expression profiles of Myf5, Esr1, Bmp4, Pax6, and Hsp70 genes during early embryonic development.
Ayper Boga Pekmezekmek, Mustafa Emre, Seyda Erdogan, Bertan Yilmaz, Erdal Tunc

Environ Sci Pollut Res Int· February 2022

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L-Glutamic acid monosodium salt reduces the harmful effect of lithium on the development of Xenopus laevis embryos.
Ayper Boga Pekmezekmek, Mustafa Emre, Erdal Tunc, Yasar Sertdemir

Environ Sci Pollut Res Int· November 2020

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Chromosomal findings and sequence analysis of target exons of calcium-sensingreceptor (CaSR) gene in patients with Sagliker syndrome.
Erdal Tunç, Osman Demirhan, Yahya Sağliker, İsmail Yildiz, Nuray Paylar

Turk J Med Sci· February 2017

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Chromosomal analyses of 1510 couples who have experienced recurrent spontaneous abortions.
Erdal Tunç, Nilgün Tanrıverdi, Osman Demirhan, Dilara Süleymanova, Nesrin Çetinel

Reprod Biomed Online· April 2016

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Microchimeric Cells, Sex Chromosome Aneuploidies and Cancer.
Deniz Taştemir Korkmaz, Osman Demirhan, Deniz Abat, Bülent Demirberk, Erdal Tunç

Pathol Oncol Res· September 2015

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Frequency and types of chromosomal abnormalities in Turkish women with amenorrhea.
Osman Demirhan, Nilgün Tanrıverdi, Erdal Tunç, Nihal Inandıklıoğlu, Dilara Süleymanova

J Pediatr Adolesc Gynecol· October 2014

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Chromosome imbalances and alterations in the p53 gene in uterine myomas from the same family members: familial leiomyomatosis in Turkey.
Sibel Hakverdi, Osman Demirhan, Erdal Tunc, Nihal Inandiklioglu, Inayet Nur Uslu

Asian Pac J Cancer Prev· July 2014

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Genetic alterations of chromosomes, p53 and p16 genes in low- and high-grade bladder cancer.
Deniz Abat, Osman Demirhan, Nihal Inandiklioglu, Erdal Tunc, Seyda Erdogan

Oncol Lett· July 2014

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Genetic polymorphisms of estrogen receptor alpha and catechol-O-methyltransferase genes in Turkish patients with familial prostate carcinoma.
Ayfer Pazarbasi, M Bertan Yilmaz, Davut Alptekin, Umit Luleyap, Zuhtu Tansug, Erdal Tunc

Indian J Hum Genet· October 2013

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Diagnosis of chromosomal abnormalities in a patient with thanatophoric dysplasia (TD) type I: The first report describing an important association between cytogenetic findings and TD.
Mehmet Turgut, Osman Demirhan, Erdal Tunc, Ibrahim Hakan Bucak, Perihan Yasemen Canoz

Am J Case Rep· April 2013

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Are there fetal stem cells in the maternal brain?
Osman Demirhan, Necmi Cekin, Deniz Taştemir, Erdal Tunç, Ali İrfan Güzel

Neural Regen Res· March 2013

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Identification of chromosome abnormalities in screening of a family with manic depression and psoriasis: predisposition to aneuploidy.
Osman Demirhan, Bülent Demirbek, Erdal Tunç, Inayet Nur Uslu, Salih Çetiner

Asian J Psychiatr· June 2012

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International evaluation of unrecognizably uglifying human faces in late and severe secondary hyperparathyroidism in chronic kidney disease. Sagliker syndrome. A unique catastrophic entity, cytogenetic studies for chromosomal abnormalities, calcium-sensing receptor gene and GNAS1 mutations. Striking and promising missense mutations on the GNAS1 gene exons 1, 4, 10, 4.
Ismail Yildiz, Yahya Sagliker, Osman Demirhan, Erdal Tunc, Nihal Inandiklioglu

J Ren Nutr· January 2012

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The genotoxic effect of nicotine on chromosomes of human fetal cells: the first report described as an important study.
Osman Demirhan, Cansun Demir, Erdal Tunç, Nihal nandıklıoğlu, Erdinç Sütcü

Inhal Toxicol· November 2011

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The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish women.
Osman Demirhan, Ayfer Pazarbaşı, Ali İrfan Güzel, Deniz Taştemir, Bertan Yilmaz, Fatma Tuncay Özgünen

Genet Test Mol Biomarkers· October 2011

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Phenotypic correlations in a patient with ring chromosome 22.
Osman Demirhan, Erdal Tunç

Indian J Hum Genet· May 2010

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Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine sampling.
Osman Demirhan, Kenan Ozcan, Deniz Taştemir, Cansun Demir, Erdal Tunç

Fertil Steril· January 2008

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