This cohort study will examine the clinical utility of genomic sequencing (GS) in patients undergoing prenatal diagnostic procedures (chorionic villus sampling or amniocentesis) for routine indications other than a structural fetal anomaly.
Pregnant Individuals Requesting Standard Microarray
This cohort study will examine the clinical utility of genomic sequencing (GS) in patients undergoing prenatal diagnostic procedures (chorionic villus sampling or amniocentesis) for routine indications other than a structural fetal anomaly.
Genomic Sequencing in Anatomically Normal Fetuses
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University of California, San Francisco, San Francisco, California, United States, 94143
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
For general information about clinical research, read Learn About Studies.
18 Years to 64 Years
ALL
Yes
University of California, San Francisco,
Mary Norton, MD, PRINCIPAL_INVESTIGATOR, University of California, San Francisco
2030-01