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Öğe A Case with Pallister-Killian mosaic syndrome(NATURE PUBLISHING GROUP, 2018) Cavdartepe, B. Eser; Kocak, N.; Cora, T.[Abstract not Available]Öğe Chromosomal Abnormalities in Mentally Retarded Children in the Konya Region - Turkey(Medecine Et Hygiene, 2000) Cora, T.; Demirel, S.; Acar, A.Etiology of mental retardation is diverse. 120 Students from 11 special training, education, and rehabilitation subclasses were investigated cytogenetically For determining the contribution of chromosomal abnormalities to mild mental retardation. 23 of the 120 children (19%) had chromosomal abnormalities: thirteen cases a classical trisomy 21 (the male: Female ratio was 9:4), three a balanced autosomal reciprocal translocation, one a pericentric inversion of chromosome 9, and six fragile-X syndrome (The male: female ratio was 5:1).Öğe Does Tarantula cubensis venom have antipoliferative & endoplasmic reticulum stress inhibitor activity on skin cancer cells?(NATURE PUBLISHING GROUP, 2019) Duran, T.; Kocak, N.; Ucar, V. B.; Cora, T.; Nergiz, S.[Abstract not Available]Öğe Effects of kras gene lcs6 mutation on metastasis pathways in human lung cancer(NATURE PUBLISHING GROUP, 2019) Azzawri, A. A.; Cora, T.; Acar, H.[Abstract not Available]Öğe Evaluation of certain protein and phosphoprotein expression levels by using western blot technique in head and neck squamous cell carcinoma(WILEY-BLACKWELL, 2016) Yigin, A. Kalayci; Cora, T.[Abstract not Available]Öğe A girl with mos45,X/46,XY/47,XYY: Genetic and clinical findings(SPRINGER, 2009) Cora, T.; Acar, H.; Atabek, E.; Balasar, Oe.; Nergis, S.[Abstract not Available]Öğe Impact of cross-talk between laryngeal cancer cells and endothelial cells on cell migration and interactions(NATURE PUBLISHING GROUP, 2019) Sari, Z. B.; Yavuz, E.; Cora, T.[Abstract not Available]Öğe Investigation of the effect of colchicine on endoplasmic reticulum stress in FMF patients(NATURE PUBLISHING GROUP, 2018) Cora, T.; Kocak, N.; Cavdartepe, B. Eser; Zainalbden, H. A.; Nergiz, S.[Abstract not Available]Öğe Mild phenotype of a large partial 13q trisomy due to t(9;13)(NATURE PUBLISHING GROUP, 2018) Cora, T.; Kocak, N.; Cavdartepe, B. Eser; Celik, S.[Abstract not Available]Öğe A novel mutation in the TCOF1 gene in a patient with Treacher Collins syndrome(NATURE PUBLISHING GROUP, 2019) Cavdartepe, B. Eser; Kocak, N.; Yasa, N.; Cora, T.; Duymus, F.[Abstract not Available]Öğe A Partial Trisomy 15q Due to 15;17 Translocation Detected by Conventional Cytogenetic and Fish Techniques(Medecine Et Hygiene, 2000) Cora, T.; Acar, H.; Oran, B.We report a case having multiple abnormalities including the simultaneous presence of the heart defect and central nerve system abnormalities, which has been reported in a few cases, and with a partial trisomy 15q. Partial trisomy 15q has been inherited from a balanced translocation carried by his phenotypically normal father, detected by traditional banding and fluorescence in situ hybridization (FISH). Application of FISH using whole chromosome specific library probes, locus specific and repetitive probes allowed us to detect the translocation between chromosomes 15q and 17q. Simultaneous application of probes revealed the position of the translocation. interestingly, in addition to the chromosomes 15 pericentromeric signals, the use of chromosome 15 beta-satellite III probe demonstrated an extra signal on chromosome 14 in both metaphase, and lighted three signals interphase nuclei which was inherited from his father. This patient is compared with other partial trisomy 15q patients reported in the literature. The results are also discussed in relation to genetic counselling for the possible relation of chromosome abnormality and clinical findings.
