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Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
- Hung, Chia-Cheng, Lin, Chia-Hui, Lin, Shin-Yu, Shin, Jin-Chung, Lee, Chien-Nan, Su, Yi-Ning
- Gene 2012 v.495 no.2 pp. 178-182
- fetus, nucleic acid hybridization, trisomics
- Trisomy 12p syndrome is a rare chromosomal abnormality, which presents with facial dysmorphism, moderate to severe psychomotor retardation and generalized hypotonia. Here we present the prenatal sonographic findings investigated of a fetus in prenatal diagnosis with a de novo trisomy of 12p identified by array-comparative genomic hybridization (aCGH).