Trisomy 18q: 46,XX,-10,+der (10) t (10;18) (p15;q12) pat: a case report
Murthy, S.K.; Kar, B.; Prabhakara, K.; Krishnamurthy, D.S.
Annales de Genetique 35(3): 174-177
1992
ISSN/ISBN: 0003-3995 PMID: 1466569 Document Number: 394061
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.