Prenatal Genetic Diagnosis by Genomic Sequencing: A Prospective Evaluation (H-45161)
Description
Content
The study will determine, in a sequential population of pregnancies with selected fetal structural anomalies and a negative or non-causal chromosomal microarray (CMA), the frequency of pathogenic, likely pathogenic, and uncertain genomic variants identifiable by sequencing.
Contact
Phone 1: 832–826–4783
IRB: H-45161
Status:
Active
Created:
