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- [2] Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21 European Journal of Human Genetics, 2009, 17 : 454 - 466
- [10] 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 CLINICAL CASE REPORTS, 2018, 6 (07): : 1313 - 1316