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Fertility and Sterility|September 21, 2007
Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine samplingOsman Demirhan, Kenan Ozcan, Deniz Taştemir, et al.The American Journal of Case Reports|April 10, 2013
Diagnosis of chromosomal abnormalities in a patient with thanatophoric dysplasia (TD) type I: The first report describing an important association between cytogenetic findings and TDMehmet Turgut, Osman Demirhan, Erdal Tunc, et al.Oncology Letters|June 25, 2014
Genetic alterations of chromosomes, p53 and p16 genes in low- and high-grade bladder cancerDeniz Abat, Osman Demirhan, Nihal Inandiklioglu, et al.Journal of Anatomy|June 6, 2022
Modifications of the locomotor system in habitually quadrupedal humansChristine Tardieu, Osman Demirhan, Eylül Akbal, et al.Asian Pacific Journal of Cancer Prevention : APJCP|April 30, 2013
Chromosome imbalances and alterations in the p53 gene in uterine myomas from the same family members: familial leiomyomatosis in TurkeySibel Hakverdi, Osman Demirhan, Erdal Tunc, et al.Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|February 23, 2015
Gene mutations in chronic kidney disease patients with secondary hyperparathyroidism and Sagliker syndromeOsman Demirhan, Ahmet Arslan, Yahya Sagliker, et al.Genetic Testing and Molecular Biomarkers|June 25, 2011
The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish womenOsman Demirhan, Ayfer Pazarbaşı, Ali İrfan Güzel, et al.Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|December 20, 2007
International study on Sagliker syndrome and uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic kidney disease patientsYahya Sagliker, Vidya Acharya, Zhang Ling, et al.Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|December 28, 2011
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, 4Ismail Yildiz, Yahya Sagliker, Osman Demirhan, et al.Pageof 4