A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype

Perçin, E. FerdaSungu, Y. SelmaRuhi, Hatice IlginErgur, Ayça TörelDüzcan, FüsunSezgin, İlhan2024-10-262024-10-2620001300-0144https://hdl.handle.net/20.500.12418/26934[No abstract available]eninfo:eu-repo/semantics/closedAccesspartial trisomy; translocation; Trisomy 13A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat KaryotypeArticle3043803772-s2.0-84888037542Q3