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- W2388444531 abstract "Fetal hypoevolutism,abnormity,fetal death,miscarriage and other congenital anomalies are due to some internal reasons,e.g chromosome micro deletion,repeat,aneuploid and so on.Array comparative genomic hybridization(Array CGH) uses array to replace traditional metaphase chromosome as target crossing to samples and reference DNA labeled by different fluorescence,and the copy number alterations are detected by analysis of different fluorescence intensity.Array CGH is a powerful tool for cytogenetical study,and it has been used in prenatal diagnosis and congenital anomalies research for abnormal microarchitecture." @default.
- W2388444531 created "2016-06-24" @default.
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- W2388444531 date "2010-01-01" @default.
- W2388444531 modified "2023-09-26" @default.
- W2388444531 title "The Application of Array CGH in Congenital Anomalies Research and Prenatal Diagnosis" @default.
- W2388444531 hasPublicationYear "2010" @default.
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