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Trisomy 18q: 46,XX,-10,+der(10) t(10;18) (p15;q12) pat: a case report
S K Murthy1, B Kar, K Prabhakara
1Department of Zoology, University School of Sciences, Gujarat University, Ahmedabad, India.
Annales De Genetique
|January 1, 1992
Abstract:
A 2-month-old female with intrauterine and postnatal growth retardation, multiple congenital anomalies, absent right kidney, congenital heart disease was investigated. Her karyotype revealed, 46,XX,-10,+der(10), t(10;18) (p15;q12) pat. The child died at 2 months 2 weeks. This is the third case of trisomy 18q resulting from translocation of chromosome 10 and 18.