1 articles published in Selcuk Medical Journal with the keyword "konjenital sağırlık": A case who has de novo 46,XY,t(13:20)(q22;p13) karyotype and congenital deafness
AYŞEGÜL ZAMANİ, HATİCE GÜL DURSUN, SENNUR DEMIREL, AYNUR ACAR
2002, Vol 18, Issue 4, Page 253-255
De novo 46:XY,t(13;20)(q22;p13) karyotype was detected in a 27 year old congenital deafness case who was referred to our laboratory because of reproductive wastage. Effect of gamets with unbalanced karyotypes which dependent on discussed balanced reciprocal translocation on reproductive vvastage...
Resiprokal translokasyon pedigri analizi Reciprocal translocation congenital deafness pedigri analysis
