Yazar "Yiğit S." için listeleme
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Chromosomal abnormalities in cases with congenital malformations
In this study we have investigated the chromosomal constitution of patients with congenital malformations in order to determine chromosomal anomaly frequencies. The conventional GTG banding patterns were routinely employed ... -
Chromosomal abnormalities in couples with recurrent pregnancyloss
Recurrent miscarriages affect approximately 5% of couples trying to establish a family. In this study we have investigated the chromosomal constitution of couples of with recurrent pregnancy losses in order to determine ... -
Results of amniocentesis cytogenetic analysis between 2000 and 2005 years at Samsun and around
Kara N.; Ökten G.; Güneş S.Ö.; Koçak I.; Yiğit S.; Tural Ş.; Pinarli F.A. (2005)In this study, we aimed to present of the results cytogenetic analysis and amniocentesis indications between the years 2000 and 2005 at Samsun and around. In this study 530 pregnancies were investigated. Each patient had ... -
Triploidy syndrome with 69,XXX karyotype: Case report [69,XXX karyotipli triplodi sendromu]
Triploidy is a chromosomal abnormality characterized by the presence of an additional haploid set of chromosomes. Triploidy is estimated to occur in 3% of conceptions. Most triploids are aborted spontaneously in the first ... -
Two Turner syndrome patients with the mosaic 45,X/46,X,i(Xq) karyotype: Case report [45,X/46,X,i(Xq) karyotipe sahip i?ki mozaik Turner sendromu olgusu]
Turner's syndrome is one of the most common chromosomal aneuploidy disorders. Turner's syndrome occurs in 1 in 4000 live-born girls and approximately 5 to 10 percent of them have mosaic isochromosome 45,X/46,X,i(Xq). ...