Browsing by Author "Pinarli, Ferda Alparslan"
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An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion
Kara, Nurten; Okten, Gulsen; Gunes, Sezgin Ozgur; Saglam, Yaman; Tasdemir, Haydar Ali; Pinarli, Ferda Alparslan (Elsevier Science Bv, 2008)Ring chromosomes are rare chromosome disorders that arise usually de novo. Children with ring chromosome 6 have a wide range of intellectual functioning and congenital anomalies. We report an epileptic case of a 10-year-old ...