Browsing by Author "Balkan, M."
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Chromosome heteromorphisms are more frequent in couples with recurrent abortions
Akbas, H.; Isi, H.; Oral, D.; Turkyilmaz, A.; Kalkanli-Tas, S.; Simsek, S.; Balkan, M. (Funpec-Editora, 2012)Chromosomal heteromorphism is considered a variant of a normal karyotype, but it is more frequent in couples with repeated miscarriages. We investigated chromosomal heteromorphism in couples with repeated miscarriages in ... -
Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey
Balkan, M.; Akbas, H.; Isi, H.; Oral, D.; Turkyilmaz, A.; Kalkanli, S.; Simsek, S. (Funpec-Editora, 2010)We reviewed cytogenetic studies performed on 4216 patients who were referred to the Cytogenetics Unit at Dicle University Hospital, Diyarbair, Southeast Turkey, between 2000 and 2009. The cases were grouped according to ... -
Cytogenetic and clinical study of a male infant with ambiguous genitalia
Oral, D.; Balkan, M.; Duran, H.; Oen, A.; Alp, M. N.; Budak, T. (Springer, 2007)[Abstract Not Available] -
Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey
Balkan, M.; Tekes, S.; Gedik, A. (Springer/Plenum Publishers, 2008)In view of the genetic risks for the next generation, the importance of careful evaluation of karyotypes and AZF microdeletions in male infertility prior to assisted reproduction is evident. In the present study, it is ... -
Evaluation of clinical and cytogenetic findings on 1,068 second-trimester amniocenteses in Southeast Turkey
Balkan, M.; Akbas, H.; Kalkanli, S.; Sakar, M. N.; Fidanboy, M.; Alp, M. N.; Budak, T. (7847050 Canada Inc, 2011)Objective: To investigate the indications of amniocentesis for the detection of chromosomal abnormalities among a sample of patients in Southeast Turkey. Material and Methods: Between 2004 and 2007, 1,068 second-trimester ... -
Genetics Analysis with Down Syndrome and Histopathological Examination of Buccal Epithelial Cells
Kalkanli, S.; Simsek, S.; Balkan, M.; Akbas, H.; Isi, H.; Oral, D.; Turkyilmaz, A. (Soc Chilena Anatomia, 2013)Down syndrome is primarily caused by trisomy of chromosome 21. We reviewed cytogenetic studies performed on 1048 patients who were referred to the Cytogenetics Unit at Dicle University Hospital, Diyarbakir, Southeast Turkey, ... -
MicroRNA-related gene polymorphisms and idiopathic azoospermia
Balkan, M.; Ay, O. I.; Erdal, M. E.; Rustemoglu, A.; Atar, M.; Hatipoglu, N. K.; Yildiz, I. (Wiley-Blackwell, 2016)[Abstract Not Available] -
No association between catalase (CAT) gene polymorphisms and susceptibility to vitiligo in a Turkish population
Akbas, H.; Dertlioglu, S. B.; Dilmec, F.; Balkan, M. (Soc Editrice Univ, 2013)Background and Aims. Vitiligo is an acquired hypomelanotic skin disorder resulting from the loss of functional melanocytes from the cutaneous epidermis. Low catalase (CAT) activity and Accumulation of hydrogen peroxide ... -
Recessive Complex Brachydactyly, Symphalangism, Zygodactyly and Male Infertility - not a Novel Syndrome but Caused by Linked Mutations in BMPR1B and PDHA2, a New Male Infertility Gene
Yildirim, Y.; Ouriachi, T.; Woehlbier, U.; Ouahioune, W.; Balkan, M.; Malik, S.; Tolun, A. (Nature Publishing Group, 2018)[Abstract Not Available] -
A small supernumerary marker chromosome, derived from chromosome 22, possibly associated with repeated spontaneous abortions
Balkan, M.; Isi, H.; Gedik, A.; Erdemoglu, M.; Budak, T. (Funpec-Editora, 2010)We report a phenotypically normal couple with repeated spontaneous abortions and without other clinical features. Clinical, hematological, biochemical, and endocrinological aspects of the couple did not reveal any ...