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

SL Bhola, AWM Nieuwint, Kyra Stuurman

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)
10 Downloads (Pure)
Original languageUndefined/Unknown
Pages (from-to)1313-1316
Number of pages4
JournalClinical Case Reports
Issue number7
Publication statusPublished - 2018

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