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Prenatal diagnosis of trisomy 6q25.3‐qter and monosomy 10q26.12‐qter by array CGH in a fetus with an apparently normal karyotype
Abstract
We present the prenatal case of a 12.5-Mb duplication involving 6q25-qter and a 12.2-Mb deletion encompassing 10q26-qter diagnosed by aCGH, while conventional karyotype showed normal results. The genotype-phenotype correlation between individual microarray and clinical findings adds to the emerging atlas of chromosomal abnormalities associated with specific prenatal ultrasound abnormalities.
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