{Reference Type}: Case Reports
{Title}: Incidental detection of a de novo 16p13.3 microdeletion encompassing PKD1 and a familial Yq11.223 microdeletion encompassing DAZ1 in a fetus with encephalocele on prenatal ultrasound and amniotic band syndrome.
{Author}: Chen CP;
{Journal}: Taiwan J Obstet Gynecol
{Volume}: 63
{Issue}: 3
{Year}: 2024 May
{Factor}: 1.944
{DOI}: 10.1016/j.tjog.2024.03.013