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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
Bhola, Shama L., Nieuwint, Aggie W. M., Stuurman, Kyra E.Volume:
6
Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.1563
Date:
July, 2018
File:
PDF, 940 KB
english, 2018