Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2818103 | Gene | 2012 | 5 Pages |
Abstract
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).
► Prenatal diagnosis ► De novo trisomy of 12p ► Array-comparative genomic hybridization (aCGH)
Keywords
Related Topics
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Biochemistry, Genetics and Molecular Biology
Genetics
Authors
Chia-Cheng Hung, Chia-Hui Lin, Shin-Yu Lin, Jin-Chung Shin, Chien-Nan Lee, Yi-Ning Su,