WS 322.2-2010 Technical standards of prenatal screening and diagnosis for fetal common chromosomal abnormalities and open neural tube defects Part 2:Cytogenetic prenatal diagnosis for fetal chromosomal abnormalities

Scope

This part of WS 322 stipulates the requirements for prenatal diagnosis clinical work, laboratory work, and the tracking and follow-up of prenatal diagnosis cases.
This part is applicable to healthcare institutions that have obtained qualifications for prenatal diagnosis technical services. These institutions use relevant technologies recognized by the state, such as cytogenetics, to conduct fetal chromosome examinations on pregnant women, thereby making a prenatal diagnosis of whether the fetus suffers from chromosomal diseases that can be diagnosed by current cytogenetic technologies.

Development Information

Same series standard

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