Advances in cytogenetics have allowed chromosomal diseases to be reliably diagnosed, and the application of cytogenetic techniques have further allowed chromosomal anomalies to be detected early in fetuses. This helps expecting mothers, their families, and their physicians to make informed plans and decisions.
Chromosome testing primarily involves amniocentesis or chorionic villus sampling but can also be conducted using samples of blood, umbilical cord blood, or placental tissue. At Sofiva Genomics, chromosome analysis is performed by professional and experienced technicians, and expert physicians verify all reports. In this way, Sofiva Genomics provides cytogenetically tests fetal chromosomes swiftly and accurately.
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