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Partial monosomy 15q due to de novo t(15;22)(q15;p11)
M A Mori1, L Rodriguez, I Pinel
1Spanish Colaborative Study of Congenital Malformations, ECEMC, Catedra de Anatonia II, Facultad de Medicina, Universidad Complutense, Madrid.
Annales De Genetique
|January 1, 1987
Abstract:
We report a 2-years-old infant who presented psychomotor delay and facial dysmorphic features. He has a partial monosomy of 15q resulting from de novo t(15;22)(q15;p11). Up to now three other cases with a similar 15q monosomy have been reported, but the present case is the first one with a "pure" monosomy 15q.