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Title: Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant. Author: Mohammed FM, Krishna Murthy DS, Farag TI, al-Awadi SA, al-Othman SA, Hammad I. Journal: Ann Genet; 1993; 36(3):181-5. PubMed ID: 8117067. Abstract: A 10-year-old female with right oblique inguinal hernia was investigated to exclude an XY karyotype. Chromosome analysis of peripheral blood showed 46,XX,inv(13)(p13;q11). In vitro aneuploidy was observed in two cells: a) 46,XX,inv(13), inv(13); b) 47,XX, +inv(13). Her father and three sisters were carriers for inv(13). Herein the authors review briefly familial inv(13)'s and report a new variant involving breakpoints (p13;q11).[Abstract] [Full Text] [Related] [New Search]