Shama L Bhola
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|Jul 11, 2018
A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH.Shama L Bhola, Aggie W M Nieuwint, Kyra E Stuurman
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