Difficulty in genetic counseling of an asymptomatic carrier woman with a de novo 15q13.2q13.3 microdeletion encompassing CHRNA7 and OTUD7A and recurrent 15q13.2q13.3 microdeletion in the fetus
| Autor principal: | |
|---|---|
| Formato: | Artículo |
| Lenguaje: | English |
| Publicado: |
Elsevier
2025-01-01
|
| Colección: | Taiwanese Journal of Obstetrics & Gynecology |
| Acceso en línea: | http://www.sciencedirect.com/science/article/pii/S1028455924002985 |