22q11.2 Deletion Syndrome (DiGeorge): Two cases, two outcomes. The importance of prenatal identification

22q11.2 deletion syndrome, also known as DiGeorge, is caused by a missing section of chromosome 22. It is more common than other conditions routinely screened for prenatally such as cystic fibrosis, s

Fetal RhD NIPT Patient Video - Vietnamese

Fetal RhD NIPT Patient Video - Spanish

Fetal RhD NIPT Patient Video - Russian

Fetal RhD NIPT Patient Video - Chinese

Fetal RhD NIPT Patient Video - Arabic

The Role of Genetic Testing in Pregnancy Loss

Fetal RhD NIPT: Transforming care for Rh negative pregnant patients

Until recently, there has not been a reason to diverge from the standard approach of giving Rh immune globulin to all Rh negative patients. That has changed with the introduction of fetal RhD NIPT, no

Fetal RhD NIPT Patient Video