Heterotaxy in a Fetus with Prenatally Diagnosed 15q11.2 Microdeletion Syndrome.

Autor: Wilson, Patrick L., Rubenstein, Abby, Xainfu Wang, Shibo Li, Porter, Blake
Zdroj: Journal of the Oklahoma State Medical Association; Mar/Apr2024, Vol. 117 Issue 2, p55-59, 5p
Databáze: Complementary Index