| http://www.w3.org/ns/prov#value | - karyotype analysis and amniocentesis) and carrier screening to test for birth defects or genetic defects including Choroid Plexus Cysts, trisomy 18, alpha fetoprotein (AFP), Carrier Screening, Cystic fibrosis (CF), Down syndrome, sickle cell disease, Spinal Muscular Atrophy (SMA), Tay Sachs disease, Fragile X syndrome, inherited mental retardation and Canavan disease.
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