PRENATAL DIAGNOSIS SERVICE
NIMGenetics has developed KaryoNIM® Prenatal, an array-CGH to detect, in amniotic fluid or coriónica villi samples, in less that 5 days, more than 120 constitutional syndromes associated to mental retardation and/or congenital malformations.

KaryoNIM® Prenatal is specially oriented to the detection of genetic alterations in prenatla samples with clinical repercussions, minimizing the risk of obtaining results with difficult clinical interpretation.

In those cases in which the performance of a higher density Array-CGH is deemed necessary, contact our specialists.